Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Pharmacovigilance Intern

Propharma
Propharma
0-1 years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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: Pharmacovigilance Intern

Location: India
Employment Type: Full-Time
Experience Required: Freshers welcome; up to 1 year preferred
Qualification: Post-secondary education (B.Pharm/B.Sc Life Sciences preferred)

Company Overview:
ProPharma Group has been empowering the biotech, medical device, and pharmaceutical industry for over 20 years, offering expertise across regulatory sciences, clinical research, quality & compliance, pharmacovigilance, medical information, and R&D technology. With a robust advise-build-operate model, ProPharma delivers end-to-end solutions that accelerate drug and device development while ensuring compliance and safety.

Role Overview:
The Pharmacovigilance Intern will gain hands-on exposure to global pharmacovigilance operations. This role provides practical experience in ICSR management, safety data entry, regulatory support, and literature review, supporting the safe monitoring of drugs and medical products.

Key Responsibilities:

1. Case Management & Data Entry:

  • Manage assigned mailboxes, including client communications, inbound safety reports, and internal processing.

  • Conduct duplicate searches and initial book-in of cases.

  • Enter basic data into safety databases, including patient identifiers, adverse events, and suspect drugs.

  • Perform full data entry under guidance once trained.

2. Regulatory & Literature Support:

  • Redact source documents for PHI according to company procedures.

  • Facilitate literature-related activities and assist with regulatory authority database searches.

  • Prepare draft reports for client review as needed.

3. Collaboration & Communication:

  • Work independently and collaboratively with cross-functional teams.

  • Maintain accurate documentation and adhere to SOPs, regulatory guidelines, and company policies.

  • Contribute to team efficiency through attention to detail and organizational skills.

Qualifications & Skills:

  • Post-secondary education (B.Pharm, B.Sc in Life Sciences, or equivalent preferred).

  • Strong verbal, written, and interpersonal communication skills.

  • Proficient in computer systems and keyboarding.

  • Ability to prioritize tasks, maintain accuracy, and work independently or in a team.

  • Strong attention to detail and organizational skills.

  • Freshers welcome; prior industry experience up to 1 year is a plus.

Why Join ProPharma:

  • Gain hands-on pharmacovigilance experience in a global company.

  • Work in a collaborative and inclusive environment that encourages innovation and professional growth.

  • Contribute to patient safety and drug monitoring initiatives.

  • Receive mentorship and exposure to end-to-end PV operations.

Equal Opportunity:
ProPharma celebrates diversity and fosters an environment where employees can be their authentic selves. The company is committed to equity, inclusion, and ensuring all employees feel empowered to succeed.