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Process Specialist-Cdm/Pv

2-4 years
Not Disclosed
10 June 9, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title:

Process Specialist – CDM/PV

Company:

Cognizant Technology Solutions

Location:

India (Hybrid)

Work Mode:

Hybrid (Rotational Shifts)

Compensation:

Not disclosed


Job Summary:

Cognizant is seeking a Process Specialist in CDM/PV to optimize processes within Pharma Research & Development. This hybrid role requires a keen understanding of pharmacovigilance (PV) case processing, drug safety operations, and regulatory compliance. The ideal candidate will bring 2–4 years of experience in PV operations and R&D process management, supporting global safety operations with technical expertise and data-driven insights. This opportunity is perfect for pharmaceutical professionals eager to contribute to clinical safety, process improvement, and global health outcomes.


Key Responsibilities:

  • Oversee and optimize R&D processes ensuring compliance and operational efficiency.

  • Support PV case processing with accurate documentation and safety data management.

  • Collaborate with cross-functional teams to enhance safety operations.

  • Analyze data and prepare reports to inform pharmacovigilance decisions.

  • Implement innovative solutions to improve process productivity.

  • Ensure compliance with global regulatory requirements and industry standards.

  • Maintain communication across departments for seamless process execution.

  • Monitor process performance and suggest improvements.

  • Develop and update standard operating procedures (SOPs).

  • Facilitate training programs to strengthen PV knowledge and skills.

  • Troubleshoot and resolve technical or process-related issues.

  • Engage in rotational shifts for 24/7 operational coverage.


Required Skills & Qualifications:

  • Bachelor’s degree in Pharmaceutical Sciences or a related field.

  • 2–4 years of experience in pharma R&D and PV case processing.

  • Strong knowledge of safety operations and regulatory compliance (GVP, ICH-GCP).

  • Analytical skills to interpret complex pharmacovigilance data.

  • Adaptability to rotational shifts and hybrid work environments.

  • Detail-oriented with a focus on data accuracy and quality.

  • Effective communication and cross-functional collaboration abilities.

  • Familiarity with PV software and tools for case processing.

  • Proactive approach to identifying process improvements.

  • Experience in Safety Ops and PV systems (an added advantage).


Perks & Benefits:

  • Hybrid work model with rotational shift flexibility.

  • Opportunity to work in a global pharmaceutical environment.

  • Access to continuous learning and development programs.

  • Collaborative, inclusive, and supportive work culture.

  • Be part of a Forbes-listed "World’s Best Employer 2024."


About Cognizant:

Cognizant is a global leader in professional services, driving digital transformation for top-tier clients worldwide. With over 300,000 associates, the company is renowned for its innovative approach in healthcare, life sciences, and technology-driven consulting, making it a preferred employer in the pharmaceutical and clinical research industry.


Call-to-Action:

Ready to contribute to global drug safety and pharmaceutical innovation? Apply now to join Cognizant’s high-performing pharmacovigilance and process management team!