Provide scientific leadership and direction in ViiV Healthcare clinical development programs
Drive strategy for early
and/or late-stage development programs
Accountable for the development, finalization, and amendments of study protocols
Collaborate with Operations, Clinical Pharmacology, Medical, Regulatory, and Commercial Leads
Provide scientific oversight of clinical studies and ensure regulatory reporting requirements are met
Collaborate to create evidence generation and scientific outputs

B.S. OR Masters OR Ph.D. OR Pharm.D., with 5+ years of drug development experience in the pharmaceutical industry or CRO environment
Prior drug development experience in HIV / infectious diseases
Experience with writing study protocols, informed consent forms, and clinical study reports
Experience with reviewing and interpreting clinical and scientific data
Experience in contributing to end-to-end clinical development strategy including study design, data interpretation, risk assessment, and milestone planning
5+ years leading cross-functional teams, including internal and external partners

Clinical Development Director

Key skills