Medical Director
GSK
full-time
Posted on:
Location Type: Hybrid
Location: Upper Providence • Pennsylvania • United States
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Job Level
About the role
- Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting.
- Ensures scientifically sound review and interpretation of data and management of safety issues
- Makes recommendations for the further characterization, management, and communication of safety risks.
- Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally.
Requirements
- Medical degree
- Completion of a formal postgraduate clinical training, clinical residency or specialty training
- Advanced experience in the Pharmaceutical or Biotech industry working in Pharmacovigilance, or Drug Safety
- Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post-marketing activities
- Experience with Signal Detection and safety surveillance
- Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes.
- Experience working in large matrix organizations
Benefits
- Flexible working arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
pharmacovigilancesafety evaluationrisk managementsignal detectionsafety surveillancedata interpretationclinical developmentpost-marketing activitiesdrug safetyclinical residency
Certifications
medical degreepostgraduate clinical training