Hybrid Pharmacovigilance Job at IQVIA
A rare chance has emerged for qualified professionals to step into the role of Medical Safety Director at IQVIA in Bengaluru, India. This is a full-time and hybrid position. The Hybrid Pharmacovigilance Job offers an opportunity to contribute significantly to pharmacovigilance services and medical safety projects.
About IQVIA:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organisation is dedicated to creating intelligent connections that accelerate the development and commercialisation of innovative medical treatments, ultimately improving patient outcomes and population health worldwide.
Job Details:
- Job Title: Medical Safety Director
- Location: Bengaluru, India
- Job Type: Full-time, Hybrid
- Reference Number: R1573998
Job Description:
The Medical Safety Director provides medical expertise on pharmacovigilance services across all divisions. This role involves participating in all aspects of Medical Safety’s involvement in assigned trials and standalone safety projects, with appropriate oversight from management. The Medical Safety Director also offers global project leadership and mentorship to junior medical safety staff.
Key Responsibilities:
- Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs).
- Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases.
- Serve as an internal consultant to pharmacovigilance case processing teams.
- Provide aggregate reviews of safety information, including clinical data.
- Represent findings from safety and clinical data reviews during client meetings.
- Provide medical review and edits to various regulatory reports and plans.
- Attend project meetings and contribute to Safety Monitoring Committees.
- Maintain awareness of medical-safety-regulatory industry developments.
Eligibility Criteria for the Hybrid Pharmacovigilance Job:
- A medical degree from an accredited and internationally recognised medical school.
- Three (3) years of clinical practice experience with four (4) additional years in the pharmaceutical industry.
- Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research.
- Ability to establish and meet priorities, deadlines, and objectives.
- A valid medical license from the country or region of residence is preferred.
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