Associate Medical Safety Director
Associate Medical Safety Director
IQVIA
Job description
Looking to build a career in pharmacovigilance and medical safety leadership? Explore this Associate Medical Safety Director role at IQVIA, based remotely in Bengaluru.
Company Description
IQVIA is a global company that offers clinical research services. It also provides insights and healthcare intelligence. The company helps life sciences and healthcare industries. These industries work to make new medical treatments available faster. IQVIA creates intelligent connections that help improve patient outcomes and population health worldwide. The company continues seeking diverse talent committed to innovation and real world impact.
Job Summary
This home based role provides medical expertise on pharmacovigilance services across assigned divisions. As an Associate Medical Safety Director, you will support Medical Safety's involvement on clinical trials and stand alone safety projects, with guidance from senior medical safety directors. Your work will include medical review of adverse events, safety report contributions, and cross functional support to pharmacovigilance case processing and clinical teams.
Key Responsibilities
Perform medical review of trial related adverse events and post marketing adverse drug reactions.
Review case narratives, queries, coding, expectedness, seriousness, and causality assessments.
Compose, edit, and medically review Analyses of Similar Events for expedited cases.
Serve as an internal consultant to pharmacovigilance case processing teams.
Provide aggregate reviews of safety information to maintain oversight of product safety profiles.
Contribute to signal management and benefit risk evaluation of drugs.
Support preparation of responses to health authority questions.
Review and contribute to periodic aggregate safety reports.
Contribute to safety review of study protocols and investigator brochures.
Maintain product specific knowledge, including watch lists and expectedness listings.
Lead or take part in training, audit preparation, and knowledge sharing activities.
Attend project and medical safety team meetings, representing safety findings as needed.
Provide medical escalation support for medical information and pharmacovigilance projects.
Stay updated on medical safety and regulatory industry developments.
Educational Qualification
A medical degree (MBBS/MD) from an accredited and internationally recognized medical school, with a curriculum relevant to general medical education.
Skills Required
About 3 years of clinical practice experience, such as graduate medical training.
At least 2 additional years of experience in the pharmaceutical or related industry.
An equivalent mix of education, training, and experience is also accepted.
Strong knowledge of clinical research regulations, including safety and GCP guidelines.
Good knowledge of clinical trials and the pharmaceutical research process.
Ability to synthesize and analyze data from multiple sources.
Strong written and verbal communication skills for complex clinical topics.
Salary Structure
The estimated average salary for an Associate Medical Safety Director at IQVIA in India ranges from ₹28 Lakhs to ₹32+ Lakhs per year.
Career Development
This role offers strong exposure to global pharmacovigilance and safety leadership within a respected healthcare intelligence company. IQVIA also supports long term growth through mentorship, structured training, and clear opportunities to advance into senior medical safety roles.
How to Apply
Visit our job portal and search for the Associate Medical Safety Director role in IQVIA.
Click on the job posting to read all the details about the job.
Fill in your details. Upload your updated resume.
Send your application.
Education
Bachelor's Degree
Key Skills
Market insights & trends
Salary Insights
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Hiring Trends
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