Remote Non-Clinical Job at IQVIA, Bangalore
Are you looking for a Senior Medical Safety Advisor role in Pharmacovigilance? Join IQVIA and work on advanced drug safety and clinical research projects. This Remote Non-Clinical Job at IQVIA Careers focuses on evaluating safety data and adverse event reports. You will contribute to pharmacovigilance and regulatory compliance activities. The job in Bangalore offers leadership opportunities in safety surveillance. It is ideal for doctors interested in careers in drug safety and clinical research.
About the Company:
IQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights. The company helps accelerate the development and commercialization of innovative medical treatments. With a strong global presence, IQVIA combines data science, technology, and healthcare expertise to improve patient outcomes and population health worldwide.
Job Details:
- Job Title: Senior Medical Safety Advisor
- Location: Bangalore
- Work Type: Home-based (Remote)
- Job Type: Full-time
- Job ID: R1524203
Key Responsibilities:
- Review and evaluate adverse events (AEs), serious adverse events (SAEs), and adverse drug reactions (ADRs) in this Remote Non-Clinical Job in Bangalore
- Perform medical review and coding validation of clinical data
- Prepare and review safety reports such as AOSE, DSUR, RMP, and PBRER
- Provide medical expertise to pharmacovigilance teams
- Support safety surveillance and signal detection activities in this Remote Non-Clinical Job at IQVIA Careers
- Act as an internal consultant for safety-related projects
- Participate in regulatory compliance and audit preparation
- Lead and support training, knowledge sharing, and team development
- Contribute to protocol and safety documentation review
- Provide 24-hour medical support when required
Educational Requirements for this Job:
- Medical degree from a recognized institution
- Valid medical license (preferred)
Skills Required:
- Minimum 3 years of clinical practice experience
- 2 years of pharmaceutical or pharmacovigilance experience (preferred)
- Strong knowledge of pharmacovigilance and safety reporting
- Understanding of GCP and ICH guidelines
- Experience with safety databases and clinical data review
- Strong analytical and decision-making skills
- Excellent verbal and written communication
- Ability to work in cross-functional teams
- Proficiency in Microsoft Office tools
Benefits of the Remote Non-Clinical Job:
- Opportunity to work with a global leader in clinical research
- Remote work flexibility
- Exposure to advanced pharmacovigilance and safety systems
- Leadership and career growth opportunities
- Collaborative and knowledge-driven environment
- Competitive salary and benefits
- Opportunity to contribute to global patient safety initiatives
