PHARMACOVIGILANCE

Our detailed, goal-oriented team members manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring tasks.

WHY JOIN OUR MEDICAL PHARMACOVIGILANCE TEAM?

Advancement and superior training

Bring your life science, nursing or pharma experience to PPD. We’ll take it from there — taking you on a journey of professional growth through extensive training and development, and a clear ladder of progression — with full leadership support.

Dynamic environment

Expand your knowledge and experiences working on different trials through all stages of drug development with management and oversight of all contracted services. You will schedule and manage many tasks and deliverables independently over varying periods.

Culture of innovation

We encourage innovation and look to the individual contributor to drive forward change and impact processes directly. Our “bright idea” system empowers you to be inventive in your approach and interact with stakeholders to arrive at the best solution.

Strong global team

We are optimistic and resilient in our investigation of risk-benefit ratios. We adopt our clients’ perspectives, anticipate their needs and deliver quality results while bending the cost and time curve of drug development.

WHAT ROLE MIGHT BE RIGHT FOR YOU?

  • Safety administrator and specialist
  • Safety reporting administrator and specialist
  • Safety administrator manager
  • Manager, director and assistant director
  • Medical director

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