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Pharmacovigilance Scientist - Position Code: Pvs001

0-2 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

 

Pharmacovigilance Scientist – Chandigarh

Location: Chandigarh, India
Experience: 0–2+ years (Pharmacovigilance experience preferred)
Work Mode: On-site
Job Type: Full-time
Salary Range: Not specified


Job Summary:

We are seeking a Pharmacovigilance Scientist to join our team in Chandigarh to manage pharmacovigilance activities including case processing, SAE analysis, aggregate safety report writing, and signal detection. This role is suited for professionals with a Master’s in Life Sciences or a degree in Dentistry or Veterinary Sciences. If you’re looking to build a career in drug safety and regulatory compliance, apply now and contribute to the safety surveillance of both human and veterinary medicinal products.


Key Responsibilities:

  • Process and analyze Adverse Events (AEs) and Serious Adverse Events (SAEs)

  • Prepare aggregate safety reports including PBRERs, PSURs, Addendum to Clinical Overviews, PADERs, and line listings

  • Conduct quality control reviews of safety documents and regulatory submissions

  • Assist in signal detection activities and cumulative safety data evaluations

  • Utilize web-based pharmacovigilance applications and internal safety databases

  • Interpret medical data and write concise, medically accurate narratives and summaries

  • Ensure adherence to global regulatory guidelines and client-specific conventions


Required Skills & Qualifications:

  • Master’s in Life Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics)

  • OR Dentistry (BDS), Veterinary Sciences (B.V.Sc./M.V.Sc.)

  • Strong knowledge of medical terminology and pharmacovigilance regulations

  • Proficient in MS Office (Word, Excel, PowerPoint) and Windows 7/10

  • Excellent English communication – both written and verbal

  • Analytical ability to interpret and evaluate medical data

  • Prior pharmacovigilance experience preferred but not mandatory

  • Experience with safety databases and web-based applications is an advantage


Perks & Benefits:

  • Opportunity to work on global pharmacovigilance projects

  • Exposure to a wide range of aggregate report types and signal detection processes

  • Supportive learning environment for life sciences professionals

  • Structured training programs for career advancement

  • Be part of a growing, quality-focused drug safety team


Company Description:

The employer is a global healthcare and pharmacovigilance solutions provider specializing in drug safety, regulatory writing, and signal detection analytics. Known for delivering high-quality services to the pharmaceutical, biopharma, and veterinary health industries.


Work Mode:

On-site – Chandigarh, India


Call to Action:

If you hold a life sciences or veterinary degree and have a passion for drug safety and regulatory science, this is your opportunity to step into the field of pharmacovigilance. Apply now and become a vital part of a team committed to ensuring medication safety worldwide.