Associate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)
Core
Leads the development, evaluation, planning, and execution of clinical studies for drug candidates in cardiovascular, metabolic, and renal disease areas, ensuring scientific integrity and data interpretation.
Role type
Senior IC clinical scientist (Associate Director)
Builds
Clinical development programs for early and late-stage drug assets
Domain
Pharmaceutical clinical drug development (Cardiovascular, Metabolic, Renal)
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Global clinical trial management, study design, clinical research methodology, medical writing, regulatory compliance (FDA/EMEA/ICH/GCP), therapeutic area expertise, cross-functional leadership, data safety monitoring
Preferred skills
Process improvement, mentoring junior staff, strategic proposal development, external stakeholder presentation
Technologies
Clinical Study Reports, Expanded Synopsis, Medical Monitoring Plans, SAPs, Informed Consents
Responsibilities
Design and complete clinical research studies, author and review clinical trial protocols and amendments, lead planning for external stakeholder meetings, perform clinical/medical data review and safety monitoring, promote consistent data review techniques, mentor junior team members
Seniority
Senior, hands-on IC with leadership responsibilities
