Director – Medical Safety
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time | Hybrid
Experience Required: 10+ Years (Clinical + Medical Safety)
Job ID: R1515587
Job Overview
IQVIA, a global leader in clinical research services, healthcare intelligence, and advanced analytics, is seeking an accomplished Director – Medical Safety to join its growing pharmacovigilance and patient safety leadership team. This senior medical role is responsible for providing strategic and scientific oversight of medical safety activities across clinical development and post-marketing programs, ensuring compliance with global regulatory standards and best practices in patient safety.
The role requires strong clinical acumen, deep knowledge of pharmacovigilance regulations, and the ability to lead multidisciplinary teams while partnering closely with internal stakeholders and global clients.
Key Responsibilities
Provide medical leadership and strategic oversight for safety and medical monitoring activities across clinical trials and post-marketing programs.
Ensure compliance with global, regional, and local safety regulations, including ICH-GCP, pharmacovigilance guidelines, and applicable health authority requirements.
Serve as a subject matter expert on medical safety, adverse event evaluation, and risk management.
Provide expert medical review and consultation on safety cases, aggregate safety reports, risk management plans, and signal evaluation activities.
Partner with cross-functional teams including clinical operations, regulatory affairs, data management, and biostatistics to support safe and compliant study execution.
Support the development, implementation, and continuous improvement of medical safety processes, standards, and governance frameworks.
Lead and mentor medical safety professionals, supporting performance management, capability development, and succession planning.
Contribute to project planning, financial oversight, and resource management for safety programs.
Build and maintain effective relationships with internal stakeholders, sponsors, and external partners.
Required Knowledge, Skills, and Abilities
Strong knowledge of global and local regulations governing clinical research, pharmacovigilance, and medical safety.
In-depth understanding of clinical trial design, drug development, and the pharmaceutical research lifecycle.
Demonstrated ability to manage competing priorities, meet deadlines, and deliver high-quality outcomes in a fast-paced environment.
Proven leadership, financial management, and project management capabilities.
Excellent communication and interpersonal skills, with the ability to provide expert consultation across multiple projects.
Ability to establish and maintain productive working relationships with global teams, senior leadership, and clients.
Qualifications & Experience
Medical degree (MBBS or equivalent) from an accredited and internationally recognized medical school.
Minimum 5 years of post-qualification clinical practice experience, including residency or equivalent graduate medical training.
At least 5 years of experience in medical safety, pharmacovigilance, or medical monitoring within the pharmaceutical, biotech, CRO, or related healthcare industry.
Combination pathways acceptable, including clinical practice plus experience as a pharmaceutical physician.
Active and valid medical license (or equivalent) in the country of residence and practice.
Experience working in global or multi-regional clinical development environments is highly desirable.
Physical & Work Requirements
Extensive use of telephone, email, and virtual communication tools requiring clear verbal and written English communication.
Regular use of computer systems and keyboard for extended periods.
Ability to sit for prolonged durations during work hours.
Willingness to travel up to approximately 10%, based on business and client requirements.
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. By creating intelligent connections across data, technology, and analytics, IQVIA accelerates the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
Equal Opportunity Employer
IQVIA is committed to creating a diverse and inclusive workplace. All qualified applicants will receive consideration for employment without regard to race, religion, gender, age, national origin, disability, sexual orientation, gender identity, veteran status, or any other protected characteristic.
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