Global Clinical Program Lead, Cvrm

AstraZeneca

Base: $280,895 - $421,342; bonus/equity: short-ter...
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Design, conduct, monitoring clinical trials
Data interpretation and reporting
Patient safety on study level
** AstraZeneca is seeking a Global Clinical Program Lead for their Cardiovascular and Renal Metabolism (CVRM) division, focusing on the design and oversight of clinical trials. The ideal candidate will possess a medical degree or a doctorate in a scientific discipline, along with significant clinical research experience, particularly in cardiology or metabolic diseases. The role offers a competitive salary, bonuses, and a flexible working environment. **

Job Summary

  • As a Global Clinical Program Lead, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives.
  • The successful GCPL in Late Phase CVRM 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, as well as allow for the intended label indication in markets globally.
  • 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, focusing on the design and oversight of clinical trials. The ideal candidate will possess a medical degree or a doctorate in a scientific discipline, along with significant clinical research experience, particularly in cardiology or metabolic diseases. The role offers a competitive salary, bonuses, and a flexible working environment. **

Salary

Base: $280,895 - $421,342; Bonus/Equity: short-term incentive bonus opportunity, equity-based long-term incentive program; Benefits: qualified retirement program [401(k) plan], paid vacation and holidays, paid leaves, health benefits

Skills & Requirements

Must-have

  • design, conduct, monitoring clinical trials
  • data interpretation and reporting
  • patient safety on study level
  • medical expert accountabilities
  • strategic medical and scientific knowledge

Nice-to-have

  • understanding of R&D
  • bold thinking
  • unleash bold thinking
  • inspire life-changing medicines

Key Requirements

  • 3+ years clinical research expertise
  • Graduate of recognized school of medicine
  • Graduate of scientific doctorate
  • Good knowledge of biostatistics
  • Good knowledge of global regulatory environment
  • Good knowledge of pharmacovigilance

Work Rights

Not specified

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