What are the responsibilities and job description for the Clinical Project Manager position at Grove Technical Resources, INC?
Job Title: Clinical Project Manager – Investigator Initiated Studies
Location: Acton, MA (Remote/Hybrid available)
Contract: 6 Months
Type: W2
Overview:
Seeking an experienced Clinical Project Manager to oversee and coordinate Investigator Initiated Studies (IIS) within the Medical Affairs department for a leading medical device company.
Key Skills & Responsibilities:
- Manage study device requests, data, and documentation for IIS.
- Collaborate cross-functionally with R&D, Manufacturing, Engineering, and Cloud teams to ensure smooth study execution.
- Oversee project timelines, resource allocation, and budget estimation.
- Prepare reports, presentations, and study summaries for management.
- Ensure all contracts and agreements are executed per compliance.
- Support clinical operations and maintain shared documentation systems.
Qualifications:
- Bachelors in biomedical engineering or Life Sciences.
- 3–7 years of experience in medical device or pharma clinical projects.
- 2 years of project management experience.
- Strong communication, analytical, and organizational skills.
- Familiarity with regulatory guidelines and clinical documentation.
Bonus: Experience in diabetes therapeutics or biomedical engineering preferred.
Remote flexibility with occasional travel.
