Senior Director, Global Clinical Program Lead
$288,059–$432,089 year
On-site · Boston, Massachusetts, United States
Job Summary
Senior Director, Global Clinical Program Lead responsible for design, conduct, monitoring, data interpretation and reporting of late-phase CVRM clinical trials, delivering medical information to regulators and ethics committees, and serving as a GlobalClinical Head delegate across studies. Leads study design, risk assessment, safety surveillance, and authoring of core study documents; collaborates with Product Teams, regulators, investigators, and cross-functional partners; requires medical/Pharmaceutical Medicine doctorate with 3+ years of clinical research experience, strong biostatistics knowledge, and global regulatory expertise. Fluency in English and demonstrated leadership and cross-functional collaboration are essential.
Required Qualifications
- Graduate of a recognized school of medicine with an M.B.B.S., M.D. degree or equivalent, and/or a graduate of a scientific doctorate (e.g. PhD or PharmD) or equivalent in a scientific discipline or Pharmaceutical Medicine
- 3+ years clinical research expertise in relevant therapy area in study design, protocol development, monitoring and implementing clinical trials
- Good knowledge of biostatistics, global regulatory environment and pharmacovigilance
- Fluent in oral and written English
- Leadership qualities with collaborative working skills
- Strong presentation and communication skills
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