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documentation gcp microsoft office vendor management clinical trials📋 Description
- Remote role with quarterly SF visits.
- Leads clinical study teams from concept to protocol.
- Ensures GCP compliance, study quality, and timely delivery.
- Manages vendors/CROs and internal CRAs/CTAs.
- Prepares, reviews, and approves key study documents.
- Coordinates study materials and site activities per SOPs.
🎯 Requirements
- Bachelor's degree in science; advanced degree preferred.
- 8+ years in biopharma with clinical trials; 2+ years leading trials.
- Vendor management experience in clinical operations.
- Strong verbal and written communication; strategic direction.
- Ability to build cross-functional relationships.
- MS Office proficiency; willingness to travel periodically.
🎁 Benefits
- Market-leading compensation
- 401(k) with employer match
- ESPP (Employee Stock Purchase Program)
- Pre-tax commuter benefits (transit/parking)
- Flexible paid time off and holidays
- Comprehensive medical, dental, and vision coverage
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