Director Clinical Science
Director Clinical Scientist
Salary: $220,000 - $250,000
Boston, MA (Hybrid)
Job Description
EPM is partnered with a clinical-stage biotech company that is creating innovative therapeis to treat patients within the cardiovascular space. With a robust pipeline spanning 6 indications across all stages of development, extensive financial runway, and tried and true leadership in the space, this is a unique opportunity to get in with a high potential pharmaceutical company at the ground floor and help grow their teams. Working directly with the Head of Clinical Development, you have the ability to learn from one of the best in the industry and advance greatly in your career.
Responsibilities
- Serve as the lead clinical scientist on the trial team, overseeing specific aspects of clinical and scientific execution for clinical protocols
- Help in developing program strategy including clinical development plan and generate KOL relationships
- Work cross functionally with various departments to develop protocols and related study materials (e.g., informed consent forms, amendments), and coordinate with Clinical Operations on study deliverables
- Ensure case report forms (CRFs) are designed to align with protocol requirements, working closely with Clinical Data Management and Programming
- Collaborate across functions to monitor clinical data, ensuring the quality, completeness, and integrity of trial conduct
Qualifications
- 12+ years of experience with a Bachelor's degree, or 10+ years with a postgraduate degree
- 5+ years of experience in the cardiovascular space required
- Experience in clinical drug development, or a PhD, Pharm D, or RN degree is preferred
- Strong knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
- Ability to manage multiple priorities with effective planning, time management, and prioritization skills
- Scientific expertise to propose, design, and execute clinical research and development studies, and author documents related to clinical trials (e.g., medical monitoring plans, statistical analysis plans, informed consent forms, clinical study reports)
- Ability to interact with key stakeholders across Clinical Development functional areas
- Proactive approach, strategic thinking, and leadership in driving clinical study goals
Benefits
- Medical
- Dental
- Vision
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