Clinical Research Project Manager
About The Position
The Clinical Research Project Manager manages multiple clinical research studies and directly hires and supervises Clinical Research Coordinators. The role serves as a key liaison among sponsors, IRBs, core laboratories, site principal investigators, and study staff at all levels. It coordinates trial initiation and patient recruitment, and expedites project approval and study start-up. The position also participates in developing and maintaining project standard operating procedures, develops advertising strategies to support recruitment, and oversees budget management and subcontracts with associated institutions. The role supervises study staff operations, writes operations manuals, participates in formulating study policies and procedures, prepares Case Report Forms, coordinates multi-center trials, and reports study progress at investigators' meetings. Patient care is not required. The position is onsite at 60 Blossom Street, scheduled for 40 hours per week on the day shift.
Requirements
- Bachelor's degree in a related field required; experience cannot be substituted for a degree.
- 5–7 years of research-related experience required.
- Ability to make independent, effective decisions.
- Strong organizational and communication skills.
- Ability to effectively supervise and train staff.
- Strong database management and computer skills.
- Demonstrated analytical skills and ability to solve problems effectively.
- Strong budget management skills.
Nice To Haves
- Master's degree in a related field preferred.
- 1–2 years of supervisory experience preferred.
Responsibilities
- Manage multiple clinical research studies.
- Directly hire, supervise, train, and oversee the operations of study staff, including Clinical Research Coordinators.
- Serve as a key liaison with sponsors, IRBs, core laboratories, site principal investigators, and study staff.
- Coordinate trial initiation and patient recruitment, and expedite project approval and study start-up.
- Participate in developing and maintaining standard operating procedures and formulating study policies and procedures.
- Develop advertising strategies to support recruitment activities.
- Oversee budget management and subcontracts with associated institutions.
- Write operations manuals.
- Prepare Case Report Forms.
- Coordinate multi-center trials with NIH, FDA, and private foundations.
- Report study progress at investigators' meetings.
Benefits
- Comprehensive benefits
- Career advancement opportunities
- Differentials, premiums, and bonuses as applicable
- Recognition programs
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What This Job Offers
Job Type
Full-time
Career Level
Manager
