Global Development Medical Director
Core
Design, conduct, monitor, and interpret clinical trials for Cardiovascular, Renal, and Metabolic diseases to determine compound benefits/risks and support global label indications.
Role type
Senior Global Development Medical Director (Late Phase)
Builds
Clinical study protocols, safety reports, and regulatory submissions for cardiovascular, renal, and metabolic therapies.
Domain
Pharmaceutical / Clinical Research / Cardiovascular, Renal, Metabolic
Required skills
Clinical trial design, medical safety surveillance, regulatory communication, protocol development, statistical analysis plan creation, investigator meeting leadership, clinical study reporting
Preferred skills
Clinical research expertise in study design and protocol development, credibility in scientific and commercial environments
Technologies
GCP, Clinical Study Reports, Safety Monitoring Plans
Responsibilities
Provide strategic medical support for clinical study design and execution; deliver medical information to regulators and investigators; oversee medical and ethical components including patient safety; conduct safety surveillance and adverse event reporting; approve Clinical Study Reports; guide investigator-initiated trials.
Seniority
Senior, hands-on IC