IQVIA Hiring for Associate Medical Safety Director Job in India to provide expert pharmacovigilance leadership across global clinical trials and safety projects.
IQVIA, one of the world’s leading organizations in clinical research, healthcare analytics, and pharmaceutical intelligence, has announced vacancies for the position of Associate Medical Safety Director. This full-time role is open across two key locations in India—Bangalore and Ahmedabad. The job posting was published recently and remains open for applications until 31st December 2025, giving eligible candidates ample time to apply. IQVIA Hiring for Associate Medical Safety Director Job
As a global leader in life sciences, IQVIA supports the development of innovative medical treatments through deep analytics, advanced technologies, and comprehensive research services. The Associate Medical Safety Director plays a central role in ensuring the safety and regulatory compliance of clinical trials and post-marketing activities. This role involves extensive medical oversight, ensuring the accuracy, quality, and regulatory compliance of all safety assessments. IQVIA Hiring for Associate Medical Safety Director Job
If you are a medical professional with strong experience in clinical practice as well as the pharmaceutical industry, this role offers a remarkable opportunity to shape global drug safety standards and contribute to large-scale medical advancements. IQVIA Hiring for Associate Medical Safety Director Job
Job Overview
The Associate Medical Safety Director provides medical expertise in pharmacovigilance and contributes to multiple safety-related processes and documentation across clinical trials and post-marketing safety functions. The role requires strong oversight across assigned projects, expert clinical interpretation of safety data, and regulatory knowledge to ensure compliance with global safety standards. IQVIA Hiring for Associate Medical Safety Director Job
This role collaborates with multidisciplinary teams, provides guidance to case processing units, attends safety-related meetings, and contributes medical input to safety reports and regulatory submissions. The selected candidate may also act as a global safety physician or a backup safety physician on assigned studies. IQVIA Hiring for Associate Medical Safety Director Job
Key Responsibilities and Essential Functions
The Associate Medical Safety Director handles core medical and scientific responsibilities related to drug safety and oversees safety deliverables throughout the project lifecycle. IQVIA Hiring for Associate Medical Safety Director Job
1. Medical Review of Adverse Events and Safety Data
The role consists of reviewing and clarifying trial-related Adverse Events (AEs) and post-marketing Adverse Drug Reactions (ADRs). This includes:
- Reviewing narrative content
- Providing clinical annotations
- Assessing seriousness and expectedness
- Determining causality
- Ensuring medical accuracy and regulatory compliance
- Coding medical terms
- Preparing company safety summaries
This task ensures that safety data is medically sound and adheres to global pharmacovigilance standards.
2. Safety Report Authoring and Review
The Associate Medical Safety Director participates in drafting and reviewing a wide range of regulatory safety documents, including:
- IND Annual Reports
- EU Periodic Benefit-Risk Evaluation Reports (PBRERs)
- EU Periodic Safety Update Reports (PSURs)
- EU Development Safety Update Reports (DSURs)
- US Periodic Reports
- Development Risk Management Plans
- EU Risk Management Plans (RMPs)
- US Risk Evaluation and Mitigation Strategies (REMS)
These deliverables require expert medical insight and are vital in maintaining the global safety profile of pharmaceutical products. IQVIA Hiring for Associate Medical Safety Director Job
3. Aggregate Safety Data Reviews
The position requires reviewing aggregate safety information, including clinical trial datasets and post-marketing signals, to detect trends, identify risks, and contribute to overall product safety assessments.
4. Safety Monitoring and Oversight
The Associate Medical Safety Director participates in safety monitoring committees, including:
- Data Safety Monitoring Boards (DSMBs)
- Safety Monitoring Committees
- Internal medical safety team meetings
The director also provides medical support and attends client meetings, presenting critical clinical and safety findings. IQVIA Hiring for Associate Medical Safety Director Job
5. Medical Support for Case Processing
The role provides medical guidance to pharmacovigilance case processing teams, ensuring accuracy in case triage, medical evaluation, and regulatory compliance.
6. Coding Review and Data Quality Checks
Key responsibilities include reviewing coding related to:
- Adverse events
- Medical history
- Concomitant medications
- Other clinical data fields
This ensures consistency, accuracy, and alignment with medical dictionaries such as MedDRA.
7. Protocol and Study Document Review
The Associate Medical Safety Director reviews:
- Clinical trial protocols
- Investigator’s Brochures (IDB)
- Case Report Forms (CRFs)
- Project Safety Plans
- Medical Monitoring Plans
This ensures that all safety components are appropriately designed and captured as per regulatory expectations.
8. Regulatory and Medical Escalation Support
The role provides:
- 24-hour medical support for escalations
- Guidance for medical information projects
- Support for EU Qualified Persons for Pharmacovigilance (QPPV)
9. Compliance with Medical Safety Timelines
Ensures that all assigned safety deliverables are completed within regulatory, operational, and contractual timelines.
10. Maintaining Knowledge and Industry Awareness
The role demands staying updated with:
- Global pharmacovigilance regulations
- Good Clinical Practice guidelines
- Medical-safety updates
- New regulatory frameworks and safety methodologies
Eligibility Criteria and Required Qualifications
IQVIA has outlined the following qualifications for the Associate Medical Safety Director role:
1. Educational Requirements
- Medical degree (MBBS or equivalent) from an accredited and internationally recognized medical school.
- Valid medical license preferred.
2. Professional Experience
- Minimum three years of clinical practice experience, such as residency or equivalent medical training.
- Minimum two years of experience in the pharmaceutical industry, preferably in pharmacovigilance, clinical research, or medical affairs.
- Equivalent combinations of education and experience may also be considered.
3. Required Knowledge and Skills
- Strong understanding of Good Clinical Practice (GCP)
- Knowledge of pharmacovigilance regulations
- Understanding of clinical trial methodology and processes
- Ability to manage deadlines, priorities, and multiple projects
- Experience in providing expert consultation
- Strong communication and interpersonal skills
- Ability to work collaboratively with cross-functional teams
About IQVIA
IQVIA is a global leader in the life sciences industry, known for integrating advanced analytics, cutting-edge technology, and unparalleled domain expertise. The company supports biopharmaceutical clients, medical device companies, hospitals, and research organizations worldwide. IQVIA Hiring for Associate Medical Safety Director Job
IQVIA contributes to modern medical advancements by enabling data-driven research, accelerating drug development, and improving healthcare delivery. Its diverse workforce collaborates globally to deliver innovative solutions, making IQVIA a preferred employer for professionals in medical safety, clinical research, and healthcare analytics. IQVIA Hiring for Associate Medical Safety Director Job
How to Apply for the Associate Medical Safety Director Position
If you meet the eligibility criteria and are interested in pursuing this senior medical safety role, follow the steps below: IQVIA Hiring for Associate Medical Safety Director Job
Step 1: Visit the Official Job Page
Go to the official IQVIA careers portal.
(As per instructions, URLs are not reproduced in the rewritten post.)
Step 2: Search for Job ID R1497935
Use the job requisition ID R1497935 to locate the exact job opening.
Step 3: Review Requirements Carefully
Read through all the responsibilities, qualifications, and expectations before applying.
Step 4: Prepare Your Application Documents
- Updated resume
- Medical degree certificates
- Valid medical license
- Proof of clinical experience
- Previous industry experience records
- Cover letter (recommended)
Step 5: Submit Your Application Online
Complete the online form and upload all required documents.
Step 6: Monitor Email for Updates
IQVIA typically communicates interview schedules, assessments, and next steps via email.
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
