[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Informed consent is a fundamental aspect of human subjects research, but this concept involves much more than a signed consent document. In this workshop, participants will become familiar with research consenting regulations, institutional requirements, and best practices. Participants will also learn tips and tricks for creating accessible, effective consent documents and conducting successful consent conversations through a mix of interactive lectures and practical, hands-on activities.
This workshop is designed to help participants…
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident, or fellow involved in the research consenting process, including: writing consents, conducting consent conferences, and/or the training and oversight of others assigned to perform consent functions.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
This course will be in person only.
All sessions will take place from 8:00 AM – 12:30 PM.
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[/vc_column_text][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[/vc_column_text][/vc_column][/vc_row]
The goal of this workshop is to enable interaction with content experts and provide tips, templates and tools for successful financial management of clinical trials. This content will be presented by members of the MCW CTO and other experienced research professionals.
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Informed consent is a fundamental aspect of human subjects research, but this concept involves much more than a signed consent document. In this workshop, participants will become familiar with research consenting regulations, institutional requirements, and best practices. Participants will also learn tips and tricks for creating accessible, effective consent documents and conducting successful consent conversations through a mix of interactive lectures and practical, hands-on activities.
This workshop is designed to help participants…
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident, or fellow involved in the research consenting process, including: writing consents, conducting consent conferences, and/or the training and oversight of others assigned to perform consent functions.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
This course will be in person only.
All sessions will take place from 8:00 AM – 12:30 PM.
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
The goal of this workshop is to enable interaction with content experts and provide tips, templates and tools for successful financial management of clinical trials. This content will be presented by members of the MCW CTO and other experienced research professionals.
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Informed consent is a fundamental aspect of human subjects research, but this concept involves much more than a signed consent document. In this workshop, participants will become familiar with research consenting regulations, institutional requirements, and best practices. Participants will also learn tips and tricks for creating accessible, effective consent documents and conducting successful consent conversations through a mix of interactive lectures and practical, hands-on activities.
This workshop is designed to help participants…
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident, or fellow involved in the research consenting process, including: writing consents, conducting consent conferences, and/or the training and oversight of others assigned to perform consent functions.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
This course will be in person only.
All sessions will take place from 8:00 AM – 12:30 PM.
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Informed consent is a fundamental aspect of human subjects research, but this concept involves much more than a signed consent document. In this workshop, participants will become familiar with research consenting regulations, institutional requirements, and best practices. Participants will also learn tips and tricks for creating accessible, effective consent documents and conducting successful consent conversations through a mix of interactive lectures and practical, hands-on activities.
This workshop is designed to help participants…
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident, or fellow involved in the research consenting process, including: writing consents, conducting consent conferences, and/or the training and oversight of others assigned to perform consent functions.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
This course will be in person only.
All sessions will take place from 8:00 AM – 12:30 PM.
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
The goal of this workshop is to enable interaction with content experts and provide tips, templates and tools for successful financial management of clinical trials. This content will be presented by members of the MCW CTO and other experienced research professionals.
[/vc_column_text][vc_empty_space]Register now for the upcoming session on April 3rd[vc_empty_space][vc_column_text]
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow wishing to learn about clinical trial financial management, focusing primarily on industry-sponsored trials.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
This session will run from 8:00 AM – 2:00 PM. Refreshments will be available throughout the day and lunch will be provided.
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][vc_empty_space height=”20px”][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Informed consent is a fundamental aspect of human subjects research, but this concept involves much more than a signed consent document. In this workshop, participants will become familiar with research consenting regulations, institutional requirements, and best practices. Participants will also learn tips and tricks for creating accessible, effective consent documents and conducting successful consent conversations through a mix of interactive lectures and practical, hands-on activities.
This workshop is designed to help participants…
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident, or fellow involved in the research consenting process, including: writing consents, conducting consent conferences, and/or the training and oversight of others assigned to perform consent functions.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
This course will be in person only.
All sessions will take place from 8:00 AM – 12:30 PM.
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
The goal of this workshop is to enable interaction with content experts and provide tips, templates and tools for successful financial management of clinical trials. This content will be presented by members of the MCW CTO and other experienced research professionals.
[/vc_column_text][vc_empty_space]Register now for the upcoming session on April 3rd[vc_empty_space][vc_column_text]
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow wishing to learn about clinical trial financial management, focusing primarily on industry-sponsored trials.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
This session will run from 8:00 AM – 2:00 PM. Refreshments will be available throughout the day and lunch will be provided.
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][vc_empty_space height=”20px”][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Successful conduct of clinical research depends on the research team’s ability to navigate the many complexities of local and federal regulations, site logistics, and clinical operations.
[/vc_column_text][vc_empty_space height=”15px”]Register for the Upcoming May Session![vc_empty_space height=”15px”][vc_column_text]Developing a sound understanding of these issues and acquiring the ability to accurately fulfill all responsibilities is essential. It can be difficult for study teams to obtain correct and complete information and training they need to accomplish the above.
Therefore, the CTSI Academy and the Clinical Trials Office (CTO) are offering a Bootcamp Clinical Research Training Program. This program has a strong focus on the practical conduct of clinical research at MCW and its partner institutions. The goal of this program is to provide research staff – both coordinators and PIs – with important information on the research environment at MCW and its partners, while sharing tips and tools for the safe, efficient, ethical, and compliant conduct of research.
This program is made possible by contributions from experts at the MCW Office of Research, Children’s Wisconsin IRB, the departments of medicine and pediatrics and the Cancer Center and MCW Clinical Trials Offices.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident or fellow either new to clinical research or new to the MCW, CW, and VA research environments. Staff that have taken this training in the past can attend to refresh content matter and changes that occur over time.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
The Bootcamp Clinical Research Training Program is a two-day program that runs from 8:00 a.m. – 12:45 p.m. each day.[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” el_class=”box” z_index=””][vc_column][vc_column_text]
[/vc_column_text][vc_empty_space][/vc_column][/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_empty_space height=”20px”][vc_column_text]
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern”][vc_column][vc_column_text]
Informed consent is a fundamental aspect of human subjects research, but this concept involves much more than a signed consent document. In this workshop, participants will become familiar with research consenting regulations, institutional requirements, and best practices. Participants will also learn tips and tricks for creating accessible, effective consent documents and conducting successful consent conversations through a mix of interactive lectures and practical, hands-on activities.
This workshop is designed to help participants…
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
Any staff, faculty member, resident, or fellow involved in the research consenting process, including: writing consents, conducting consent conferences, and/or the training and oversight of others assigned to perform consent functions.
[vc_separator type=’normal’ position=’center’ color=’ffffff’ thickness=’2′ up=’12’ down=’14’]
This course will be in person only.
All sessions will take place from 8:00 AM – 12:30 PM.
A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.
Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).
[/vc_column_text][/vc_column][/vc_row]
