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gcp excel powerpoint edc ms word📋 Description
- Coordinate clinical study operations from startup to closeout across projects
- Develop study documents: protocol, informed consent, training materials
- Manage vendor contracting, budgeting, invoicing with minimal oversight
- Support CDM in CRFs and EDC testing
- Maintain filing and archiving of clinical documents per SOPs
- Oversee biospecimen supplies tracking and storage
🎯 Requirements
- BA/BS in life sciences or related field
- Minimum 4 years experience in clinical studies (academic/biopharma/diagnostics)
- Experience with clinical EDC systems
- Familiarity with TMF structure and processes
- Proficiency in MS Word, Excel and PowerPoint
- Knowledge of SOPs, ICH-GCP, and FDA regulations
🎁 Benefits
- Medical, dental, vision, life and disability plans
- Free cfDNA testing for employee and dependents; fertility benefits
- 401k plan and commuter benefits
- Employee referral program
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