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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Lead the scientific strategy behind clinical studies from design through execution and reporting
- Partner with Medical Directors and cross-functional teams to shape protocols, amendments, and study conduct
- Build expertise in disease biology, compound mechanism of action, and the competitive treatment landscape
- Author and review expanded synopses, monitoring plans, study reports, and other key trial documents
- Safeguard patient safety through ongoing clinical and medical data review
- Identify risks to study integrity and drive mitigation strategies
- Represent Clinical Sciences on program teams, steering committees, and safety monitoring boards
- Champion consistent, high-quality data review practices across assigned studies
Requirements
What you’ll need- MS, PhD, or PharmD in a related scientific field
- 8+ years of pharmaceutical clinical drug development experience
- Experience in Immune/Inflammatory clinical trials preferred
- Knowledge of GCP, ICH guidelines, clinical trial design, and regulatory requirements
- Strong medical writing skills
- Expertise in clinical research methodology
- Demonstrated success working cross-functionally in a matrix organization
Benefits
Comp & perks- Annual bonuses or other incentive plans
- Equity awards
- Pension or retirement benefits
- 401(k) company match
- Health and wellness programs
- Fitness centers
- Medical, dental, vision, life, and disability insurance benefits
- Paid time off
- Family support benefits
- Reasonable accommodation during the recruitment process where required