Global Development Medical Director
Core
Design, conduct, monitor, and interpret late-phase clinical trials for Cardiovascular, Renal, and Metabolic diseases to determine benefits, risks, and global label indications.
Role type
Senior IC Global Development Medical Director
Builds
Clinical studies and medical data packages for late-phase drug development
Domain
Pharmaceutical R&D, Cardiovascular, Renal, and Metabolic diseases
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Study design, protocol development, clinical trial monitoring, data interpretation, regulatory compliance, safety surveillance, statistical analysis, investigator meeting management
Preferred skills
Nephrology or NASH expertise, pharmaceutical industry R&D knowledge, drug development milestone understanding
Technologies
Clinical Study Report, Statistical Analysis Plan, Case Report Forms, Safety and Risk-Based Monitoring Plans
Responsibilities
Accountable for study designs and medical aspects; drive study team decisions; ensure patient safety and GCP compliance; deliver study documents; manage safety surveillance and adverse event reporting; approve Clinical Study Reports; educate study team members; collaborate with global colleagues and external partners.
Seniority
Senior, hands-on IC