Medical Advisor Job at IQVIA | Careers in Pharmacovigilance – MBBS Graduates Apply Now!
IQVIA Careers presents an excellent medical advisor job opportunity for experienced doctors seeking growth beyond traditional clinical roles. This full-time, home-based position in Bengaluru focuses on pharmacovigilance, medical safety evaluation, and regulatory compliance, making it a strong option among medical jobs and high-demand jobs in Bangalore within the global life sciences industry.
Job Details:
- Job Position: Senior Medical Safety Advisor
- Location: Bengaluru, India (Home-based | Full-time)
- Job ID: R1524203
About the Company:
IQVIA is a global leader in advanced analytics, clinical research, and technology solutions for the life sciences sector. Through IQVIA careers, medical professionals gain access to impactful roles that support drug safety, regulatory science, and improved patient outcomes worldwide.
Qualifications:
- Medical degree from an accredited and internationally recognized medical school
- Minimum three (3) years of clinical practice experience after the award of the medical degree
- Two (2) years of pharmaceutical industry experience preferred
- Equivalent experience in clinical practice or pharmacovigilance may be considered
- Strong knowledge of medicine and pharmacovigilance processes
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements
- Experience with ICSR and aggregate safety reports
- Familiarity with SOPs and multiple safety databases
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong verbal and written communication skills
- Ability to work effectively with cross-functional teams and regulatory agencies
- Valid medical license in the country or region of practice
Job Description:
The objective of this medical advisor job is to provide 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. This position also serves as a senior technical leader, participating in matrix management activities, evaluation of safety issues, preparation of aggregate reports, and surveillance activities in collaboration with Post-Marketing Safety Experts and the Safety Surveillance Group.
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)
- Provide coding review of AEs, SAEs, SADRs, past medical history, and concomitant medications
- Serve as an internal consultant to pharmacovigilance case processing teams
- Conduct medical safety review of protocols, Investigator Brochures, and Case Report Forms (CRFs)
- Perform aggregate safety reviews, including DSURs, RMPs, PBRERs, and regulatory reports
- Ensure service delivery from productivity, compliance, and quality perspectives
- Provide pharmacovigilance guidance while leading safety team members
- Maintain watch lists, expectedness lists, labeling lists, and RSIs
- Lead training, product transitions, audit preparation, and knowledge exchange initiatives
- Review and sign off on Project Safety Plans and Medical Monitoring Plans
- Act as Lead Safety Physician or provide backup support
- Provide medical escalation support and 24-hour medical coverage as required
