**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

**Job Description**

Join us as **Manager PVG** – And lead the efforts in managing and optimizing drug safety operations to ensure the highest standards of patient safety and regulatory compliance in clinical trials.

**What You’ll Do:**

+ Manage multiple aspects of projects, both local and globally, such as contractual, procedural and regulatory requirements.
+ Maintain good communications with other functional groups concerning program and company issues. Collaborating with other employees in problem solving and systems improvement.
+ Review regulatory/pharmacovigilance publications and information sources to keep updated on current regulations, practices, procedures and proposals.
+ Maintain a basic medical understanding of applicable therapeutic areas and disease states. May participate in on-call duties for specific projects and ensure 24...