Opportunity Description
**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...
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...
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