Pharmacovigilance ICSR Specialists

Pharmazone ICSR Specialist Recruitment

Pharmazone is hiring experienced ICSR Specialists to join its expanding Pharmacovigilance team.

The recruitment includes 4 open positions for professionals with relevant experience in ICSR and Pharmacovigilance.

Candidates with 3–6 years of experience in ICSR or Pharmacovigilance and strong case-processing knowledge can apply.

The positions are for immediate joiners only and involve end-to-end safety case processing, coding, narrative writing, and quality compliance.

ICSR Specialist

Department: Pharmacovigilance – ICSR

Vacancies: 4 Positions

Experience: 3–6 Years

Eligibility & Qualifications

B.Pharm | M.Pharm | Pharm.D | M.Sc. Life Sciences | M.Sc. Pharmacology | M.Sc. Biotechnology | M.Sc. Biochemistry | Clinical Research

Key Responsibilities

End-to-End ICSR Processing

• Perform end-to-end ICSR case processing from intake through submission.
• Handle both serious and non-serious safety cases within defined timelines.
• Ensure accurate and timely processing of safety information.

Case Assessment & Documentation

• Perform case assessment and data entry.
• Prepare case narratives.
• Perform medical coding as required.
• Support medical review activities.

Quality & Compliance

• Conduct quality and compliance checks.
• Ensure adherence to applicable Pharmacovigilance regulations.
• Follow established SOPs and quality standards.
• Maintain compliance with defined case-processing timelines.

Required Skills

ICSR Case Processing | Pharmacovigilance | Case Assessment | Data Entry | Narrative Writing | Medical Coding | Safety Case Processing | PV Regulations | SOPs | Quality Compliance

Immediate Joining

Immediate Joiners ONLY

How to Apply

Interested and eligible candidates can share their updated CV at

Email: hr@pharmazones.com

Job Summary

Company

Pharmazone

Vacancies

ICSR Specialist – 4 Positions

Required Education

Not Specified; relevant courses include B.Pharm, M.Pharm, Pharm.D, M.Sc. Life Sciences, Pharmacology, Biotechnology, Biochemistry, Clinical Research

Experience

3–6 Years in ICSR / Pharmacovigilance

Tagged as: Case Processing, Clinical Research, Documentation, ICSR, Medical Review, Pharmacovigilance