- Pay: $50-61/hr.
- 100% remote position.
- 3-month assignment with possibility for extension or conversion based on performance and budget.
- Program & Trial Leadership – Translate scientific concepts into study designs, integrate biomarkers/digital health initiatives, contribute to protocols/training materials, oversee trial execution, ensure data integrity, and support regulatory responses.
- Scientific & Clinical Oversight – Provide expert input into development plans, assess/select biomarkers/endpoints, lead adjudication/data visualization activities, review data for quality, and oversee study closure/reporting.
- Collaboration & Vendor Management – Liaise with investigators, KOLs, and consultants; partner with data sciences, statistics, regulatory, and operations; oversee vendor integration of data/technology.
- Safety Management – Contribute to medical review planning, participate in data review meetings, prepare safety monitoring summaries, and support IDMC activities.
- External Communication & Publications – Support DEI strategy, contribute to publications, scientific presentations, and external communications on clinical findings.
- PhD/MD/PharmD with 1-2 years of relevant work experience or Master’s degree with 2-4 years is required
- Background and ability to take scientific concepts and translate and implement them into the clinical study design and/or for clinical study planning and execution is required
- Background in biomarkers / digital technologies and or data science initiatives is required