Note: The job is a remote job and is open to candidates in USA. EPM Scientific is recruiting for an unnamed client. The Director will lead clinical science for clinical-stage CVRM programs, supporting study execution, medical monitoring, site engagement, and clinical trial design.
Responsibilities
- Serve as clinical science lead and core member of clinical development team for clinical stage CVRM programs
- Support day-to-day study execution, ensuring alignment with protocol, timelines, and regulatory requirements
- Participate in medical monitoring activities: review and interpret clinical data on an ongoing basis in collaboration with cross-functional colleagues and external partners to ensure data quality, participant safety, and protocol compliance. Escalate issues as appropriate
- Participate in site selection, initiation, and ongoing engagement; provide scientific support to investigators and address protocol-related inquiries
- Design and develop clinical trial protocols and associated documents (e.g. clinical study plans, data review plans, case report forms (CRFs), database design, statistical analysis plans) in collaboration with CMO
- Collaborate with clinical & non-clinical teams to ensure alignment
Skills
- MD or PhD; and 5+ years of industry experience in clinical development
- Experience with cardio, metabolic or related disease areas required
- Demonstrated ability to lead clinical science strategy and execution in early-stage trials
- Strong critical thinking and problem-solving skills
- Good team player, excellent communication skills, learning agility
- Proven ability to collaborate across geographies (U.S., China, Australia) and functions (R&D, BD, regulatory) in matrixed environments
- Strong analytical and decision-making skills to translate scientific insights into actionable clinical strategies
- Gene therapy experience preferred
Benefits
- Remote (US); must be based in PST
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