Clinical Research Program Manager

## Clinical Research Program Manager Apply remote type:
Onsite locations:
Boston-MAtime type:
Full time posted on:
Posted Todayjob requisition :
RQ4074606

Site:
The Brigham and Women's Hospital, Inc.

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.
** Job Summary
** The Cancer and Well-being Research Program (CARE) at Brigham and Women’s Hospital is  recruiting a full-time Clinical Research Program Manager to join its multidisciplinary team. The  program manager will work closely with the principal investigator in collaboration with a  diverse group of researchers (oncologists, palliative care clinicians, psychiatrists, psychologists)  to oversee the day-to-day administration of program activities. The program manager will  contribute to the development of study protocols and procedures, and the preparation and  submission of research manuscripts, abstracts, and grant applications.

The program manager  will be responsible for hiring and onboarding new staff as well as maintaining a working  knowledge of clinical research conduct to support study-related activities and initiatives across  the program locally and nationally.
** Qualifications
* * Education  Qualifications  
• BA/BS degree required  
• Master’s degree or PhD preferred  
• Minimum of 5 years of research experience preferred  
• Minimum of 2 years of management experience required    Knowledge,

Skills and Abilities

• Collaborate with the principal investigator to oversee all laboratory projects  
• Work closely with the principal investigator on grant submissions, including summarizing  grant instructions and required elements, assisting with writing research proposals,  developing templates for required documents, and collecting required documentation  from investigators and study sites  
• Assist with manuscript preparation for peer-reviewed journals, including performing  literature reviews, outlining study methods and findings, and editing manuscripts prior to  submission  
• Assist with abstract and presentation submissions for local, regional, national, and  international conferences  
• Assist with writing protocols for CARE studies, including Institutional Review Board  applications and informed consent documents, as well as defining project timelines and  maintaining study amendments and continuing reviews  
• Collaborate with the principal investigator to develop standard operating procedures and  templates to improve efficiency and consistency across all studies  
• Oversee all Institutional Review Board communications regarding projects  
• Monitor progression of clinical trials against project milestones  
• Oversee all study procedures, compliance, and communication with all collaborating  institutions for multi-site trials  
• Oversee all data collection in collaboration with clinical research coordinators for accuracy  and compliance  
• Oversee internal and external audits and coordinate all processes with Data Safety and  Monitoring Boards for all clinical trials
• Act as the point of contact for CARE members to provide direction and guidance regarding  day-to-day issues and activities as well as interpretation of hospital and regulatory policies  
• Maintain centralized training records for all research staff  
• Maintain and update CARE email distribution lists and manage the CARE meeting  schedule, including presentations, journal clubs, and guest speakers  
• Work with the Development Office to support activities for CARE donors, including Patient  Advisory Councils  
• Oversee program website to ensure content is current and accurate; manage CARE study  email accounts and respond to inquiries; submit study team reimbursements
** Additional Job Details (if applicable)
**** Remote Type
** Onsite
* * Work Location
**…