Pharmacovigilance Job at IQVIA
Looking for an experienced Pharmacovigilance Job that allows doctors to move deeper into drug and medical safety? IQVIA Careers has an opening for an Associate Medical Safety Director in Bengaluru, offered as a full-time, home-based position. Medical graduates with clinical practice and pharmaceutical industry experience can apply. Among specialised Medical Jobs India, this opportunity involves adverse-event review, aggregate safety evaluation, regulatory reporting and medical oversight of clinical 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 organization focuses on creating intelligent connections to accelerate the development and commercialization of innovative medical treatments, ultimately aiming to improve patient outcomes and population health worldwide. With a commitment to integrity, IQVIA maintains a zero-tolerance policy for candidate fraud and values honesty and professionalism in its hiring process.
Job Details:
- Position: Associate Medical Safety Director
- Reference Number: R1552764
- Location: Bengaluru, India
- Employment Type: Full-Time
- Work Model: Home-Based
- Function: Medical Safety / Pharmacovigilance
Job Description:
This Pharmacovigilance Jobs opportunity at IQVIA is for an Associate Medical Safety Director who will provide medical expertise across pharmacovigilance services. The selected professional will participate in medical safety activities for assigned clinical trials and standalone safety projects, with appropriate management oversight. Responsibilities span AE and ADR medical review, aggregate safety evaluation, regulatory documentation, client interactions and participation in Safety Monitoring Committees.
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 to maintain oversight of a product’s safety profile.
- Represent safety and clinical data review findings during client meetings.
- Provide medical review and edits to various regulatory reports and plans.
- Attend and contribute to medical safety evaluations on Safety Monitoring Committees.
- Maintain awareness of medical-safety-regulatory industry developments.
Eligibility Criteria for this Pharmacovigilance Job:
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Candidates interested in these Pharmacovigilance Jobs through IQVIA Careers should meet the following requirements:
- Medical degree from an accredited and internationally recognized medical school.
- Three years of clinical practice experience.
- Two additional years of pharmaceutical industry experience.
- Knowledge of local and federal regulations governing clinical research.
- Valid medical licence in the candidate’s country or region of residence is preferred.
- Ability to manage priorities, deadlines and project objectives effectively.
Skills Required for this Pharmacovigilance Job:
- Pharmacovigilance & Drug Safety
- AE & ADR Medical Review
- Aggregate Safety Evaluation
- Clinical Safety Data Interpretation
- Regulatory Report Review
- Medical & Scientific Assessment
- Clinical Research Regulatory Knowledge
- Communication & Stakeholder Management
