Instagram
youtube
Facebook

Process Specialist-Cdm/Pv

2-4 years
Not Disclosed
10 June 27, 2025
Job Description
Job Type: Hybrid 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 | Hybrid | Cognizant


Job Summary

Cognizant is seeking a Process Specialist – CDM/PV to join its growing pharmacovigilance and clinical data management team. This role supports Pharma Research & Development operations with a focus on safety, regulatory compliance, and process excellence. Designed for professionals with 2 to 4 years of industry experience, this hybrid role offers a dynamic work environment with rotational shifts and no travel requirements. The ideal candidate brings analytical strength, attention to detail, and technical capabilities to optimize pharmacovigilance operations.


Key Responsibilities

  • Oversee and optimize Pharma R&D processes for compliance and efficiency

  • Support pharmacovigilance case processing with accurate safety documentation

  • Collaborate with teams to enhance safety operations and workflow integration

  • Analyze safety data and create reports to support strategic decisions

  • Drive process innovation using best practices and technical insights

  • Ensure compliance with global regulatory requirements in safety operations

  • Facilitate inter-departmental communication for streamlined operations

  • Develop and maintain SOPs to ensure quality and process consistency

  • Provide training support to enhance team skills in PV and safety operations

  • Troubleshoot process issues and provide timely solutions

  • Continuously improve process quality through data-driven recommendations

  • Engage in rotational shifts to maintain 24/7 global PV support


Required Skills & Qualifications

  • Bachelor’s or Master’s in Pharmaceutical Sciences or related field

  • 2–4 years of experience in pharmacovigilance, CDM, or Pharma R&D

  • Proficiency in PV case processing and safety operations

  • Knowledge of regulatory frameworks such as GVP, ICH-GCP

  • Strong data analysis and decision-making skills

  • Familiarity with PV tools/software (e.g., Argus, MedDRA)

  • Excellent communication and collaboration abilities

  • Ability to thrive in a hybrid work environment and handle rotational shifts

  • Strong attention to detail and process optimization mindset

  • Proactive in identifying and resolving operational issues


Perks & Benefits

  • Hybrid work model with flexible rotational shifts

  • Competitive compensation package

  • Global career exposure with a leading pharmaceutical client

  • Professional development programs in pharmacovigilance and R&D

  • Inclusive and collaborative work culture

  • Access to Cognizant’s internal learning platforms and upskilling resources


Company Description

Cognizant is a globally recognized leader in pharmaceutical services, driving innovation across pharmacovigilance, regulatory affairs, and R&D operations. With 300,000+ professionals across the world, Cognizant empowers global pharma companies with digital transformation and compliance excellence. Ranked among Forbes World’s Best Employers 2024, Cognizant is trusted for its delivery, integrity, and global scale.


Work Mode:

Hybrid – India (No Travel Required)


Call-to-Action

If you are ready to take the next step in your pharmacovigilance and clinical operations career, this is your opportunity to join a world-class healthcare team at Cognizant.

Apply now to elevate your career with Cognizant’s Pharma R&D operations.