Added
less than a minute ago
Location
Type
Full time
Salary
Upgrade to Premium to se...
Related skills
documentation gcp microsoft office vendor management clinical trials📋 Description
- Lead the clinical study team for assigned projects from concept to protocol.
- Ensure GCP compliance, high study quality, and timely completion.
- Manage external vendors and CROs; coordinate internal staff (CRAs/CTAs).
- Prepare/Review/Approve study documents: Monitoring Manual, SOM, SDV Plan, Lab Manual.
- Coordinate and design study materials: CRFs, patient diaries, study participation cards, and source documents.
- Oversee operational activities at study sites to ensure adherence to GCP, SOPs, and study protocols.
🎯 Requirements
- Bachelor’s degree in a scientific discipline; advanced degree preferred.
- 8+ years in biopharma with 2+ years leading clinical trials.
- Vendor management experience in clinical operations/development.
- Strong verbal/written communication; can convey strategic direction.
- Ability to build and maintain cross-functional relationships.
- Experience with Microsoft Office Suite (Word, Excel, Project, Outlook).
- Willing to travel periodically.
🎁 Benefits
- Market leading compensation
- 401K with 100% employer match on first 3% and 50% on the next 2%
- Employee stock purchase program
- Pre-tax commuter benefits
- Referral program with $2,500 award for hired referrals
- Health care with 100% premiums covered; mental health support via Spring Health
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Healthcare Jobs. Just set your
preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!