Medical Job Opportunity at IQVIA – Associate Medical Safety Director, Apply Now!
IQVIA is offering an excellent medical job opportunity for experienced professionals in pharmacovigilance and clinical safety. This Associate Medical Safety Director role is a full-time, home-based position located in Bengaluru and is ideal for candidates looking to grow through IQVIA careers while working with global safety surveillance teams. Among the top jobs in Bangalore, this role combines leadership, regulatory expertise, and patient safety responsibilities.
Job Details:
- Job Position: Associate Medical Safety Director
- Location: Bengaluru, India
- Job ID: R1514647
About the Company:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Through innovative data-driven solutions, IQVIA careers support the development and commercialization of medical treatments that improve patient outcomes and population health worldwide. The company is widely recognized for offering high-quality medical job roles and professional growth opportunities.
Qualifications:
- Medical degree from an accredited and internationally recognized medical school
- Minimum three (3) years of clinical practice experience after a medical degree
- Two (2) years of pharmaceutical industry experience preferred
- Equivalent education, training, or experience in clinical practice, pharmacovigilance, or CRO environments may be considered
- Strong knowledge of medicine and pharmacovigilance
- In-depth understanding of GCP, ICH guidelines, and regulatory requirements
- Experience with ICSR processing and aggregate safety reports
- Familiarity with SOPs and multiple safety databases
- Valid medical license preferred
Medical Job Description:
This medical job focuses on providing medical expertise in the evaluation of safety data from multiple sources as part of the overall pharmacovigilance process. The role involves determining the medical and scientific relevance of serious adverse event reports within the context of a product’s safety profile and related therapeutic areas.
Medical Job 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
- Provide medical coding review of AEs, SAEs, SADRs, medical history, and concomitant medications
- Serve as an internal consultant to pharmacovigilance case processing teams at IQVIA
- Conduct medical safety reviews of protocols, Investigative Brochures, and Case Report Forms
- Perform aggregate safety reviews, including DSUR, RMP, PBRER, literature reviews, and observational studies
- Ensure productivity, compliance, and quality within regulatory timelines
- Provide therapeutic area guidance and lead safety team members
- Attend project and client meetings representing medical safety findings
- Provide medical escalation and EU QPPV project support
- Stay updated on global medical safety and regulatory developments
