Director, Well Managed – Business Cards & Payments
Capital One
Scientific Director
GSK
full-time
Posted on:
Location Type: Office
Location: Massachusetts, North Carolina, Pennsylvania • 🇺🇸 United States
Visit company websiteJob Level
Lead
About the role
- Responsible to lead medical and scientific staff within the SERM (Safety Evaluation & Risk Management)
- Define and drive the strategy and vision of clinical safety and pharmacovigilance activities in alignment with Global Safety business strategies
- Implement policy, processes and support the implementation of operational and strategic plans
- Ensure scientifically sound review and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process to senior management
Requirements
- Health Sciences/Health Care Professional degree required (e.g., BSc, MS, PhD, RN/BSN/MSN, NP, RPh/B Pharm/Pharm D, Dentists and Veterinarians are also accepted)
- Comprehensive experience in the Pharmaceutical or Biotech industry working in Drug Safety or Pharmacovigilance
- Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post-marketing activities
- Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes
Benefits
- Comprehensive benefits program
- Health Sciences/Health Care Professional degree required
- Comprehensive experience in the Pharmaceutical or Biotech industry working in Drug Safety or Pharmacovigilance
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
pharmacovigilancesafety evaluationrisk managementdata interpretationclinical developmentpost-marketing activitiesdrug developmentdrug approval processes
Soft skills
leadershipstrategic planningpolicy implementationcommunication
Certifications
BScMSPhDRNBSNMSNNPRPhB PharmPharm D
