- Waltham, Massachusetts, United States
- Hybrid
- Full-time · Director
- $159K–$195K per year
- 5+ years
A unique opportunity to play a key role in the research and development organization, allowing for hands-on scientific responsibility of clinical trial execution and delivery in support of a Phase 3 pivotal study slated for NDA submission.
Compensation
$159,000—$195,000 USD
Responsibilities
- Support the Medical Directors for one or more Phase I–III clinical studies
- Lead studies across the full trial lifecycle, from start-up through database lock and reporting
- Provide scientific input to the efficacy and safety endpoint objectives of clinical trials
- Identify and provide solutions to data trends, inconsistencies, and potential issues; partnering with Data Management, Biostatistics, and Safety
- Collaborate effectively with cross-functional teams including Clinical Operations, Data Management, Biostatistics, Programming, Safety, and Regulatory
Requirements
- RN
- MS
- PhD
- PharmD
- Nice to have: Advanced degree