Clinical Project Manager
Meet Life SciencesBoston, MA, United States11 hours ago
Job type
- Full-time
Job descriptionBachelor’s degree in Biomedical Engineering, Life Sciences, or related field. 3–7 years in medical device or drug-related clinical research. Minimum 2 years of project management experience. Biomedical engineering and / or diabetes therapeutic experience preferred. Strong analytical, organizational, and interpersonal skills. Knowledge of regulatory guidelines. Excellent verbal and written communication. Proficient in project management and multi-tasking. Skilled in MS Office, databases, and timeline software. Ability to communicate across all organizational levels. Flexible, detail-oriented, and a strong team player. Willingness to work on-site in Acton, MA as needed. Approximately 10% domestic / international travel.
Job Title : Clinical Project Manager – Investigator Initiated Studies
Responsibilities :
- Collaborate with Medical Affairs to manage study device and data requests.
- Work cross-functionally with Manufacturing, R&D, and Engineering to procure study devices.
- Partner with technical teams to set up remote monitoring and data exports.
- Oversee execution of agreements and contracts.
- Prioritize requests to optimize resources and timelines.
- Prepare project plans, status updates, and summary reports for management.
- Maintain and update a shared site for central project documents.
- Review protocols to determine device needs and study requirements.
- Estimate device and resource costs per study.
- Support other clinical study activities as needed.
- Perform additional duties as assigned.
Education & Experience :
Skills & Competencies :
Other Requirements :
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Clinical Project Manager • Boston, MA, United States
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