Drug Safety Physician Job at Cencora | Apply Now
A drug safety physician job is one of the most critical roles in pharmacovigilance, ensuring medicines remain safe for patients worldwide. If you are looking for MBBS jobs in Noida, the opportunity at Cencora offers a strong career path in drug safety, regulatory compliance, and safety report management. This role involves preparing safety reports, evaluating pharmacovigilance data, and collaborating with global teams to maintain regulatory standards. Professionals exploring Cencora careers can benefit from this leadership role in safety writing and drug safety evaluation.
Job Details:
- Job Position: Manager – Drug Safety Physician
- Location: Noida, India
- Job ID: R264402
- Company: Cencora
- Affiliated Company: PharmaLex India Private Limited
About the Company:
At Cencora, team members are at the heart of everything the organization does. The company is united in its responsibility to create healthier futures, and every employee contributes to delivering that mission. Through innovation and collaboration, Cencora works to improve the lives of people and animals everywhere.
Professionals exploring Cencora careers have the opportunity to work at the center of healthcare innovation while contributing to safer medicines and improved global health outcomes.
Job Description:
This drug safety physician job focuses on the development, authorship, and tracking of safety reports such as PSUR, RMP, and ACO to ensure documents are high quality, regulatory compliant, and distributed appropriately. The role also involves managing safety writing activities, mentoring employees, and overseeing service performance within pharmacovigilance operations.
The position requires collaboration with cross-functional teams to develop regulatory-compliant safety documents and ensure all reporting commitments are tracked and fulfilled according to regulatory requirements.
Qualifications:
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Educational: Degree in Medicine (MBBS / MD required)
Experience & Skills:
- Minimum 5–7 years of relevant experience in pharmacovigilance and drug safety
- Hands-on experience in medical review of Aggregate Safety reports, ICSRs, regulatory compliance, and signal detection
- Strong interpersonal and organizational skills with a collaborative mindset
- Ability to work under pressure with high responsibility and dedication
- Exposure to corporate pharmaceutical or life sciences environments preferred
- Excellent written and verbal communication skills in English
- Knowledge of safety databases, regulatory guidelines, SOPs, and literature surveillance
Key Responsibilities:
- Development, authorship and tracking of Safety Reports (PSUR/RMP/ACOs) to ensure that documents are of high quality, regulatory compliant, and that logistics and distribution are handled in an appropriate and timely manner.
- Mentoring employees enabling them to work independently within timelines, budget, and quality.
- Organize the kick off meeting, prepare PSURs & RMP’s as per the client’s SOPs and working practices.
- Ensure quality of the draft during preparation of RMP/PSUR/ACOs.
- Development and authorship of high quality and regulatory compliant PSUR-PBRER, RMP, ACO & DSURs in collaboration with required teams.
- Coordinate activities from different line units to ensure all documents required to support the RMP/PSUR/ACO main document are included in the annexes.
- Work with authors from different line functions to ensure content meets client and Health Authorities requirements.
- Update the RMP according to Health Authority requirements and ensure alignment with regulatory documents such as PSUR and CDS.
- Ensure consistency and regulatory compliance of RMP/PSUR/ACO sections and annexes.
- Track Health Authorities feedback and ensure requirements are implemented as required.
- Ensure proper maintenance of all RMP/PSUR/ACO documents as per process.
- Ensure RMP/PSUR/ACO approved by Health Authorities are dispatched as required.
- Evaluate safety database, literature, clinical trial data, and epidemiology data to address HA responses.
- Formulate strategies for safety issues, Health Authority requests, and integrated benefit-risk evaluation.
