Clinical Research Program Lead – Grants & Multi-Site Trials

The General Hospital Corporation

Boston (MA)

On-site

USD 90,000 - 130,000

Full time

6 days ago
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Job summary

The Brigham and Women’s Hospital, Inc. is recruiting a full-time Clinical Research Program Manager for the CARE program.

The role collaborates with oncologists, palliative care clinicians, psychiatrists, and psychologists to oversee day-to-day administration, develop study protocols, and support manuscript and grant activities across local and national sites. The successful candidate will manage staff onboarding, ensure compliance with clinical research conduct, and contribute to

Qualifications

  • BA/BS degree required
  • Minimum of 2 years of management experience required
  • Master's degree or PhD preferred
  • Minimum of 5 years of research experience preferred

Responsibilities

  • Oversee day-to-day administration of the CARE program activities and coordinate with the principal investigator
  • Assist with grant submissions, including summarizing instructions and gathering required documentation
  • Support manuscript preparation for peer-reviewed journals and conference submissions
  • Assist with protocol development, IRB applications, and maintaining project timelines
  • Develop standard operating procedures and templates to improve efficiency across studies
  • Coordinate data collection and ensure compliance across multi-site trials
  • Serve as a liaison for CARE staff, manage training records, and maintain study communications

Skills

Management experience

Education

BA/BS degree
Master's degree or PhD preferred

Job description

The Brigham and Women’s Hospital, Inc. is recruiting a full-time Clinical Research Program Manager for the CARE program.

The role collaborates with oncologists, palliative care clinicians, psychiatrists, and psychologists to oversee day-to-day administration, develop study protocols, and support manuscript and grant activities across local and national sites. The successful candidate will manage staff onboarding, ensure compliance with clinical research conduct, and contribute to

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