Global Clinical Program Lead, Cvrm

AstraZeneca

Base: $280,895 - $421,342; bonus/equity: short-ter...
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Global clinical program leadership
Cvrm therapy area expertise
Clinical trial design and conduct
** AstraZeneca is seeking a Global Clinical Program Lead for their Cardiovascular and Renal Metabolism (CVRM) division, responsible for overseeing clinical trials and ensuring ethical compliance while delivering impactful medical insights. The role requires a medical degree and extensive experience in clinical research, particularly in cardiology or metabolic disease, along with strong collaboration and communication skills. **

Job Summary

  • The Global Clinical Program Lead will be responsible for the design, conduct, monitoring, data interpretation and reporting of clinical trials ensuring that the clinical data collected within the study will allow determination of the benefits and risks of the compound.
  • Accountable for the medical and ethical components of studies including patient safety on a study level in compliance with GCP.
  • In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program.

Matching Summary

Match Score: 75

** AstraZeneca is seeking a Global Clinical Program Lead for their Cardiovascular and Renal Metabolism (CVRM) division, responsible for overseeing clinical trials and ensuring ethical compliance while delivering impactful medical insights. The role requires a medical degree and extensive experience in clinical research, particularly in cardiology or metabolic disease, along with strong collaboration and communication skills. **

Salary

Base: $280,895 - $421,342; Bonus/Equity: Short-term incentive bonus and equity-based long-term incentive program; Benefits: 401(k) plan, paid vacation and holidays, paid leaves, medical, prescription drug, dental, and vision coverage

Skills & Requirements

Must-have

  • Global clinical program leadership
  • CVRM therapy area expertise
  • Clinical trial design and conduct
  • Data interpretation and reporting
  • Regulatory compliance and GCP

Nice-to-have

  • Strategic medical and scientific knowledge
  • Partnership and collaboration skills
  • Cross-country and cross-culture communication
  • Understanding of R&D and drug development

Key Requirements

  • 3+ years clinical research expertise
  • M.B.B.S., M.D., PhD or PharmD degree
  • Good knowledge of biostatistics
  • Global regulatory environment knowledge
  • Pharmacovigilance knowledge

Work Rights

Not specified

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