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data analysis r python gcp edc📋 Description
- Support design and development of clinical study protocols, endpoints, criteria
- Translate research and product goals into evidence-generating study plans
- Partner to execute studies ensuring alignment between scientific intent and operational delivery
- Build relationships with internal teams, investigators, and external partners
- Prepare study documents: protocols, investigator brochures, clinical study reports, regulatory submissions
- Ensure GCP compliance and alignment with data collection strategy
🎯 Requirements
- Familiarity with statistical methods or programming (Python, R)
- 5+ years in clinical research or scientific roles in medical devices
- Strong analytical and problem-solving skills with data interpretation
- Familiarity with clinical study design, endpoints, and data analysis concepts
- Working knowledge of GCP and ISO 14155
- Ability to work cross-functionally with clinicians, engineers, and operational teams
🎁 Benefits
- Opportunity to work with leading experts from multiple fields
- Growth potential and fast-track advancement
- Medical, dental, and vision insurance
- Paid holidays
- Commuter benefits
- Equity (RSUs) for eligible full-time employees
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