Lead the scientific planning and collaborate with Clinical Research, Pharmacovigilance and Clinical Operations in the execution of clinical trials
Job Summary
Lead the scientific planning and collaborate with Clinical Research, Pharmacovigilance and Clinical Operations in the execution of clinical trials.
Contribute to evidence generation for regulatory approval and/or engagement with physicians, including protocol development, study implementation, data analysis and reporting of results.
This role requires a minimum of 3 days a week of onsite presence in either Jersey City (NJ) or Millbrae (CA) offices.
Matching Summary
Lead the scientific planning and collaborate with Clinical Research, Pharmacovigilance and Clinical Operations in the execution of clinical trials.
Skills & Requirements
Must-have
Clinical trial protocol development
Medical monitoring
Clinical data analysis and reporting
Cross-functional collaboration
GCP and ICH regulatory requirements
Nice-to-have
Data driven and collaborative integrator
Exemplary communication and presentation skills
Strategic thinking and leadership
Key Requirements
10+ years of experience with a Bachelor's degree
8+ years of experience with a post graduate degree
PhD, Pharm D, or RN degree preferred
Solid knowledge of clinical research regulatory requirements