Related skills
ms excel sops tmf ich-gcp fda regulations📋 Description
- Maintain oversight of study sample activities to meet TAT.
- Collaborate with Data Management to build dashboards and KPIs.
- Track samples from receipt to result reporting with sites/collabs.
- Anticipate, investigate, and resolve issues to ensure deliverables.
- Handle data files to support timely result reporting.
- Review study protocols for sample collection aligned with SOW.
🎯 Requirements
- BA/BS degree in life sciences or related field
- Minimum of 5 years of clinical study experience
- Familiarity with biospecimen management and biobanking
- Experience with clinical EDC systems
- Competency in SOPs, ICH-GCP, FDA Regulations
- Proficiency in MS Word, Excel and PowerPoint
🎁 Benefits
- Competitive benefits: medical, dental, vision, life, and disability
- Free testing for employees and families; fertility care
- 401k, commuter benefits, and more
- Generous employee referral program
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