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ProPharma Hiring Pharmacovigilance Specialist in India

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ProPharma

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, RPh, RN, Advanced Degree

Remote Or Hyderabad

Minimum 2 Years

Verified Job

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ProPharma has announced an exciting Pharmacovigilance Specialist recruitment opportunity for professionals with experience in Individual Case Safety Report (ICSR) processing, adverse event case management, MedDRA coding, and regulatory safety reporting. This full-time opportunity is open to candidates across India, making it an excellent career option for Pharmacovigilance professionals looking to work with a globally recognized pharmaceutical consulting organization.

If you have experience in case processing, medical narrative writing, expedited reporting, and global pharmacovigilance regulations, this opportunity offers excellent career growth while working with global pharmaceutical, biotechnology, and medical device clients.


ProPharma Pharmacovigilance Specialist Recruitment 2026 โ€“ Overview

ParticularDetails
CompanyProPharma
Job TitlePharmacovigilance Specialist
Job TypeFull-Time
LocationIndia
DepartmentPharmacovigilance
ExperienceMinimum 2 Years
QualificationBachelor’s Degree in Life Sciences
Preferred QualificationPharmD, RPh, RN, Advanced Degree
Working ModelRemote / Hybrid (Based on Location)
Job PostedAugust 7, 2026

About ProPharma

For over 25 years, ProPharma has been helping pharmaceutical, biotechnology, and medical device companies accelerate product development while maintaining regulatory compliance. The company provides end-to-end consulting services across:

  • Pharmacovigilance
  • Regulatory Affairs
  • Clinical Research
  • Medical Information
  • Quality & Compliance
  • R&D Technology Solutions

ProPharma supports organizations throughout the complete product lifecycle using its Advise-Build-Operate model.


Key Responsibilities

As a Pharmacovigilance Specialist, you will be responsible for managing the complete lifecycle of Individual Case Safety Reports (ICSRs).

Your responsibilities include:

  • Process adverse event cases from clinical trials and post-marketing sources
  • Perform MedDRA coding for adverse events
  • Assess seriousness and expectedness of safety events
  • Conduct follow-up activities to obtain missing safety information
  • Prepare and review high-quality medical narratives
  • Generate client notifications related to safety cases
  • Ensure expedited reporting compliance according to global regulations
  • Review case quality for consistency and accuracy
  • Support training activities and knowledge sharing
  • Maintain compliance with SOPs and pharmacovigilance guidelines
  • Escalate case discrepancies whenever necessary
  • Stay updated with evolving global drug safety regulations

Required Qualifications

Candidates should possess:

  • Bachelor’s Degree in Life Sciences (Mandatory)

Preferred qualifications include:

  • PharmD
  • Registered Pharmacist (RPh)
  • Registered Nurse (RN)
  • Advanced Degree in Life Sciences

Experience Required

Applicants should have:

  • Minimum 2 years of Pharmacovigilance experience
  • Hands-on experience in:
    • ICSR Case Processing
    • MedDRA Coding
    • Seriousness Assessment
    • Expectedness Assessment
    • Narrative Writing
    • Regulatory Reporting
    • Pharmacovigilance SOP Compliance

Essential Skills

Successful candidates should demonstrate:

  • Excellent written and verbal communication
  • Strong analytical thinking
  • High attention to detail
  • Case quality review expertise
  • Ability to prioritize multiple safety cases
  • Team collaboration skills
  • Knowledge of global pharmacovigilance regulations
  • Problem-solving abilities
  • Time management

Why Join ProPharma?

Working at ProPharma offers several advantages:

  • Global Pharmacovigilance exposure
  • Opportunity to work with leading pharmaceutical companies
  • Remote and hybrid work flexibility
  • Strong learning and development culture
  • Inclusive workplace environment
  • Career progression opportunities
  • Exposure to international regulatory requirements
  • Collaborative multidisciplinary teams

Who Should Apply?

This role is ideal for professionals currently working as:

  • Pharmacovigilance Associate
  • Drug Safety Associate
  • Drug Safety Specialist
  • PV Case Processor
  • Safety Scientist
  • ICSR Associate
  • Medical Reviewer
  • Pharmacovigilance Executive

Keywords for Job Seekers

  • ProPharma Pharmacovigilance Specialist Jobs
  • Pharmacovigilance Jobs India
  • Drug Safety Jobs 2026
  • ICSR Case Processing Jobs
  • Remote Pharmacovigilance Jobs
  • MedDRA Coding Jobs
  • Pharmacovigilance Specialist Vacancy
  • Life Sciences Pharmacovigilance Careers
  • Drug Safety Associate Jobs India
  • PV Specialist Recruitment

How to Apply

Application Link

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