Pharmacovigilance Intern

Why This Role Matters
The Pharmacovigilance Intern role at CliniResource provides an essential entry point into the highly regulated and critical field of drug safety and pharmacovigilance. Pharmacovigilance plays a vital role in protecting patient safety by monitoring, assessing, and reporting adverse drug reactions in compliance with global regulatory frameworks.
This internship offers fresh graduates structured exposure to real-world pharmacovigilance workflows followed by pharmaceutical companies and Contract Research Organizations (CROs). By contributing to adverse event case processing, safety documentation, and regulatory compliance activities, interns gain foundational experience that directly supports public health and regulatory transparency.
For candidates seeking pharmacovigilance internship jobs in Delhi/NCR, this opportunity strengthens industry readiness and builds the professional discipline required in global drug safety operations.

Job Description
CliniResource is offering an office-based Pharmacovigilance Internship for fresh M.Pharm, Pharm.D, and BDS graduates located in New Delhi/NCR. This role is designed to provide structured, hands-on training in pharmacovigilance case processing, adverse event reporting, and regulatory documentation practices.
The selected interns will work closely with safety and regulatory teams to process Adverse Event (AE) and Serious Adverse Event (SAE) reports, assist in Individual Case Safety Report (ICSR) documentation, maintain safety databases, and support compliance activities aligned with ICH and global pharmacovigilance guidelines.
This internship focuses on building core competencies required for entry-level drug safety and pharmacovigilance roles within pharmaceutical companies and CRO environments.

Key Features of the Role
• Structured hands-on training in pharmacovigilance operations
• Exposure to AE and SAE case processing workflows
• Practical learning of ICSR documentation procedures
• Compliance alignment with ICH and global regulatory standards
• Real-time safety database management experience
• Office-based professional learning environment
• Direct interaction with pharmacovigilance and regulatory professionals
• Foundational training for long-term drug safety careers

Responsibilities Required

• Process and review Adverse Event (AE) reports
• Assist in handling Serious Adverse Event (SAE) documentation
• Support preparation and review of Individual Case Safety Reports (ICSRs)
• Maintain accurate safety database entries and documentation records
• Assist in aggregate safety data review activities
• Ensure compliance with ICH guidelines and global pharmacovigilance standards
• Coordinate with internal safety and regulatory teams for case follow-up
• Support documentation accuracy and case tracking processes
• Maintain confidentiality and data integrity across safety workflows
• Participate in internal training and quality review sessions

Qualifications
• M.Pharm (Pharmacology or Pharmaceutics preferred)
• Pharm.D
• BDS

Educational Requirements
• Completed postgraduate or professional degree in Pharmacy or Dentistry
• Academic understanding of pharmacology, drug safety, and adverse event monitoring

Experience and Skills
• Fresh graduates are eligible
• Strong conceptual understanding of pharmacovigilance principles
• Basic knowledge of ICH guidelines and global drug safety regulations
• Good written and verbal communication skills
• Strong attention to detail and documentation accuracy
• Ability to understand and interpret medical terminology
• Structured and process-oriented working style
• Basic computer proficiency for database documentation
• Willingness to learn regulated safety workflows
• Ability to work effectively in an office-based professional setting

Salary Insights
• Estimated stipend: ₹12,000 – ₹18,000 per month
• Compensation aligned with industry standards for pharmacovigilance interns in Delhi/NCR
• Internship provides high-value industry exposure beyond monetary compensation
• Strong return on investment in terms of long-term career growth potential

Company Overview
CliniResource operates within the pharmaceutical and clinical research domain, supporting pharmacovigilance and drug safety operations. The organization focuses on providing structured training and operational exposure to fresh graduates entering regulated healthcare environments.
Through practical safety case processing, compliance documentation, and regulatory alignment, CliniResource enables early-career professionals to develop strong foundations in pharmacovigilance operations. The company emphasizes process discipline, regulatory accuracy, and professional development within a structured office-based environment.

FAQs

• Q: Is this internship remote?
A: No. This is an office-based internship located in New Delhi/NCR.

• Q: Are freshers eligible?
A: Yes. Fresh M.Pharm, Pharm.D, and BDS graduates are encouraged to apply.

• Q: Is prior pharmacovigilance experience required?
A: No prior industry experience is mandatory, but basic conceptual understanding is expected.

• Q: Will interns receive hands-on ICSR exposure?
A: Yes. Interns will assist in ICSR documentation and safety case processing workflows.

• Q: What career roles can this internship lead to?
A: This internship builds a foundation for roles such as Drug Safety Associate, Pharmacovigilance Executive, Safety Scientist, or Clinical Research professional.

• Q: Are candidates outside Delhi/NCR eligible?
A: No. Only candidates residing in Delhi/NCR are eligible.

Application Tips

• Highlight academic projects related to pharmacovigilance or drug safety
• Mention coursework in pharmacology, clinical research, or regulatory affairs
• Demonstrate understanding of AE, SAE, and ICSR concepts
• Emphasize documentation accuracy and attention to detail
• Showcase strong communication skills in your resume
• Prepare to discuss basic ICH guidelines during interviews
• Express willingness to learn structured, regulated workflows