IQVIA Careers: Apply Now for Medical Safety Advisor Position
IQVIA Careers: IQVIA is seeking an experienced senior medical safety advisor to provide expert medical oversight of global safety data, contribute to the pharmacovigilance strategy, and ensure robust safety surveillance across multiple therapeutic areas. This role is ideal for a medical professional passionate about safeguarding patient safety while influencing major post-marketing and clinical safety programs.
IQVIA Careers—Job Details
- Position: Senior Medical Safety Advisor
- Job ID: R1471135
- Location: Bengaluru, India
About the Institute
IQVIA is a global leader in clinical research, healthcare intelligence, and data-driven innovation. With advanced analytics, technology solutions, and unmatched therapeutic expertise, IQVIA accelerates the development and commercialization of life-changing medical treatments worldwide. The company is known for its collaborative culture, cutting-edge scientific environment, and commitment to improving patient outcomes and global public health.
IQVIA Careers-Qualifications
- Medical degree (MBBS or equivalent) from an accredited and internationally recognized medical school.
- Minimum 3 years of clinical practice experience after medical graduation (residency/graduate training may count).
- Preferably 2+ years of pharmaceutical/industry experience.
- Strong knowledge of general medicine and clinical safety.
- In-depth understanding of GCP, ICH guidelines, and global PV regulations.
- Knowledge of ICSRs, aggregate safety reports, and signal detection principles.
- Experience working with safety databases.
- Strong communication skills (written and verbal).
- Ability to manage cross-functional interactions with global teams, sponsors, and regulatory representatives.
- A valid medical license is preferred.
Role Overview
The Senior Medical Safety Advisor provides medical expertise in the assessment of safety data, offers scientific interpretation of adverse event reports, and collaborates closely with global pharmacovigilance teams. The role also involves senior technical leadership, mentoring team members, and ensuring compliance with regulatory timelines and quality standards.
Key Responsibilities
- Conduct medical reviews of clinical trial AEs, post-marketing ADRs, causality assessment, expectedness, seriousness, and narrative quality.
- Prepare and medically review Analyses of Similar Events (AOSE) for expedited regulatory submissions.
- Review clinical data, including AEs, SAEs, SADRs, concomitant medications, medical history, and coding accuracy.
- Serve as an internal consultant for case processing teams and PV operations.
- Review safety sections of study protocols, investigator brochures, CRFs, and related clinical documents.
- Perform aggregate safety evaluations and contribute to reports such as DSURs, RMPs, PBRERs, and ad-hoc regulatory submissions.
- Maintain oversight of product safety profiles through literature review, observational data, and clinical evidence.
- Ensure compliance with productivity standards, quality metrics, and regulatory timelines.
- Guide and support teams in safety assessments and therapeutic area decision-making.
- Maintain and update product safety watchlists, labeling lists, and RSIs.
- Lead and participate in training programs, audits, transitions, and knowledge exchange initiatives.
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