Pharmacovigilance Job at IQVIA, Bengaluru
Interested in a Pharmacovigilance Leadership Role with a Global Clinical Research Company? IQVIA is hiring an Associate Medical Safety Director for its pharmacovigilance and medical safety team in Bengaluru. This home-based opportunity is ideal for medical professionals with expertise in drug safety, adverse event review, and clinical research regulations. The Pharmacovigilance Job at IQVIA in Bengaluru involves medical evaluation of safety data, aggregate safety reporting, signal detection, and collaboration with global pharmacovigilance teams. Candidates will contribute to patient safety monitoring and regulatory compliance across clinical trials and post-marketing surveillance activities at IQVIA Careers. Professionals looking to build a long-term career in medical safety and global drug development can find strong growth opportunities in this position.
About the Company:
IQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. The company supports pharmaceutical and healthcare organizations through advanced analytics, clinical development, and pharmacovigilance solutions aimed at improving patient outcomes worldwide.
Job Details:
- Job Role: Associate Medical Safety Director
- Location: Bengaluru
- Work Mode: Home-Based
- Job Type: Full-Time
- Job ID: R1514647
- Department: Pharmacovigilance / Medical Safety
Key Responsibilities:
- Perform medical review of adverse events and adverse drug reactions
- Review narrative content, coding, seriousness, causality, and expectedness of safety cases in this Job in Bengaluru
- Prepare and review Analyses of Similar Events (AOSE) reports
- Conduct coding review for medical histories, concomitant medications, and clinical data listings
- Provide medical guidance to pharmacovigilance case processing teams at IQVIA Careers
- Support safety review of protocols, Investigative Brochures, and Case Report Forms
- Prepare aggregate safety reports such as DSUR, RMP, and PBRER
- Participate in signal detection and safety surveillance activities in this Pharmacovigilance Job
- Lead training activities, product transitions, and audit preparation
- Attend client meetings and present safety review findings
- Provide medical escalation support and 24-hour medical coverage when required
Educational Requirements for this Job:
- Medical degree from an accredited medical school
- Minimum 3 years of clinical medicine experience after a medical degree
- Pharmaceutical industry or pharmacovigilance experience preferred
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Understanding of pharmacovigilance processes and aggregate reporting
- Valid medical license preferred
Skills Required:
- Pharmacovigilance and drug safety expertise
- Clinical data review and adverse event assessment
- Knowledge of global clinical research regulations
- Medical coding and safety database handling
- Aggregate safety reporting skills
- Strong analytical and problem-solving abilities
- Excellent written and verbal communication skills
- Team collaboration and stakeholder management
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Attention to detail and compliance management
Benefits of the Pharmacovigilance Job:
- Opportunity to work with a globally recognized clinical research organization
- Exposure to international pharmacovigilance and drug safety projects
- Home-based work flexibility
- Career growth in medical safety and regulatory sciences
- Experience in aggregate safety reporting and signal detection
- Collaboration with global healthcare and research teams
- Opportunities for leadership and training responsibilities
- Involvement in advanced clinical development and patient safety programs
