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Tm-Pharmacovigilance

3+ years
Not Disclosed
10 July 8, 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

 

TM – Pharmacovigilance (Regulatory Intelligence & Safety Monitoring)

Location: India (Hybrid Work Model)
Work Mode: Hybrid (with Rotational Shifts)
Experience Level: Mid to Senior Level
Industry: Pharmacovigilance, Regulatory Affairs, Healthcare Compliance


Job Summary:

Cognizant is hiring a TM – Pharmacovigilance professional with expertise in regulatory intelligence and customer service to ensure drug safety compliance and enhance patient outcomes. This hybrid role requires strong pharmacovigilance experience, proficiency in English, and the ability to lead initiatives that integrate regulatory strategy with operational excellence.


Key Responsibilities:

  • Monitor and analyze adverse drug reactions (ADRs) to ensure safety and efficacy

  • Interpret and apply regulatory intelligence to improve pharmacovigilance operations

  • Provide PV process guidance to improve customer experience and safety protocols

  • Prepare and submit regulatory reports and maintain compliance documentation

  • Collaborate with R&D teams to integrate safety insights into product development

  • Utilize analytical tools to assess and optimize PV systems and practices

  • Conduct research for developing new PV methodologies and best practices

  • Drive process improvements and strategic initiatives in drug safety operations

  • Stay informed on global pharmacovigilance regulations and industry trends

  • Ensure communication between stakeholders and regulatory teams remains seamless

  • Lead projects that support regulatory integration into business decisions


Required Skills & Qualifications:

  • Bachelor’s or Master’s in Pharmacy (B.Pharm / M.Pharm)

  • Certified Pharmacovigilance Professional or Regulatory Affairs Certification

  • Minimum 3 years of experience in pharmacovigilance, safety monitoring, or regulatory affairs

  • Strong knowledge of regulatory guidelines (GVP, ICH, FDA, EMA)

  • Proven experience in regulatory intelligence and customer-centric PV support

  • Excellent English communication skills (verbal and written)

  • Experience in hybrid work environments with rotational shift flexibility

  • Proactive, detail-oriented, and capable of process optimization


Perks & Benefits:

  • Work with a globally recognized healthcare and life sciences leader

  • Inclusive, collaborative workplace with high-performing global teams

  • Opportunities for career advancement and skill development

  • Access to cutting-edge PV technologies and global health data systems

  • Competitive compensation (subject to role and location)

  • Recognition as one of Forbes World’s Best Employers 2024


Company Description:

Cognizant is a global leader in digital and healthcare transformation, serving the pharmaceutical and life sciences sectors with cutting-edge solutions. With over 300,000 associates globally, Cognizant delivers innovation, regulatory compliance, and operational excellence to clients worldwide.


Work Mode: Hybrid (India) | Shifts: Rotational

Preferred Salary Range: Not disclosed (subject to company and location policies)


Call to Action:

Are you a certified PV professional with regulatory expertise? Take the next step in your career with Cognizant and contribute to global drug safety initiatives.

Apply now to join Cognizant’s pharmacovigilance team and lead with purpose.