Pharmacovigilance Job at Cognizant | Medical Safety Role for Pharma Graduates

Cognizant Hiring Medical Safety Role | Pharma Graduates | Apply Online

Pharmacovigilance Job opportunities at Cognizant Careers are now open for the position of TL-Medical Safety in Noida, India. This role contributes to medical safety activities within a global pharmaceutical environment by supporting end-to-end safety case review and documentation for clinical and post-marketing products. The position operates under a hybrid work model and focuses on ensuring patient safety and regulatory compliance across diverse therapeutic areas.

About the Company

Cognizant is an AI Builder and technology services provider, bridging the gap between AI investment and enterprise value by building full-stack AI solutions for clients. Its deep industry, process and engineering expertise enables organizations to build their unique context into technology systems that amplify human potential, drive tangible outcomes and keep global enterprises ahead in a fast-changing world. See how at cognizant.ai or @cognizant.

Job Details

Job Description

• This Pharmacovigilance Job focuses on systematic medical safety review of individual case safety reports within clinical and post-marketing settings.
• The role involves end-to-end case processing, including medical evaluation, narrative refinement, coding verification, and consistency checks to maintain high-quality safety data.
• Candidates will interpret clinical trial data, product labels and risk-benefit profiles while ensuring compliance with global regulatory requirements.
• Active participation in safety review meetings and collaboration with pharmacovigilance and safety operations teams are essential to support aggregate safety assessments and regulatory submissions.

Key Responsibilities

• Perform systematic medical safety review of individual case safety reports.
• Assess seriousness, causality, and clinical relevance in alignment with global regulatory expectations.
• Execute end-to-end case processing including medical evaluation and coding verification.
• Verify source documents and supporting clinical information for completeness and coherence.
• Participate in safety review meetings and provide case-level insights.
• Adhere to pharmacovigilance workflows and standard operating procedures.
• Utilize safety databases to retrieve, analyze, and update case information.
• Contribute to signal detection and risk evaluation activities.

Eligibility Criteria

• Education: Academic background in life sciences, pharmacy, medicine or a related discipline.
• Experience: Practical experience or training in pharmacovigilance and safety operations with exposure to case processing workflows and medical review principles.
• Language: Effective communication in English through clear written and spoken interactions.

Required Skills

• Knowledge of pharma research and development processes and clinical trial phases.
• Ability to conduct structured medical safety review of individual case safety reports.
• Strong attention to detail and analytical thinking.
• Familiarity with safety databases and coding practices.
• Understanding of global pharmacovigilance regulations.
• Capability to maintain accurate documentation and audit trails.
• Collaboration skills for cross-functional team coordination.
• Adaptability to hybrid work arrangements and day shift schedules.

Certifications Required

Preferred certification in pharmacovigilance or drug safety, such as professional training in Good Pharmacovigilance Practices or equivalent industry-recognized programs.

Why Join this Role?

This role provides exposure to global pharmacovigilance operations within a hybrid work model. Professionals will strengthen their expertise in individual case safety report assessment, regulatory compliance, and signal detection activities. The position supports continuous learning in evolving pharmacovigilance regulations and medical safety methodologies, enabling contributors to enhance patient safety outcomes and build strong competence in safety review practices across therapeutic areas.

CLICK HERE TO APPLY ONLINE

Biotecnika is a career information portal and is not the recruiter for this position. All details are sourced from the official notification. Candidates should verify eligibility and deadlines on the official website before applying.