Pharmaceutical - Internship (WFH & Part Time)

About the internship:Selected intern's day-to-day responsibilities include:

Arzon Global is looking for motivated and detail-oriented Pharmacovigilance Interns to join our Drug Safety team. This internship provides practical exposure to pharmacovigilance, adverse drug reaction (ADR) reporting, safety data review, case processing, and drug-safety documentation.

The ideal candidate should have a basic understanding of medicines and pharmacology, strong attention to detail, good documentation skills, and an interest in pursuing a career in pharmacovigilance or the pharmaceutical industry.

1.Assist the pharmacovigilance team in reviewing and documenting Adverse Drug Reaction (ADR) information.

Support the identification and collection of relevant safety information from available sources.

Assist with Individual Case Safety Report (ICSR) data entry and case documentation under supervision.

Review case information for completeness, consistency, and accuracy.

2.Assist in identifying important patient, drug, and adverse-event information from case narratives.

Support the documentation and maintenance of pharmacovigilance records.

Assist with basic case follow-up activities and information tracking as assigned.

Support medical literature review activities related to drug safety, where applicable.

3.Assist in maintaining safety databases, spreadsheets, and relevant documentation.

Follow standard operating procedures (SOPs) and data-quality requirements.

Maintain confidentiality of patient and safety-related information.

Support the team in preparing reports, trackers, and other pharmacovigilance-related documentation.

Perform other drug-safety and pharmacovigilance activities assigned by the supervisor.Who can apply:Only those candidates can apply who:are available for the work from home job/internshipcan start the work from home job/internship between 10th Oct'26 and 14th Nov'26are available for duration of 3 monthshave relevant skills and interests* Women wanting to start/restart their career can also apply.Stipend:INR₹ 6,000 - 15,000 /monthDeadline:[hidden]:59:59Other perks:Certificate, Letter of recommendation, Flexible work hoursSkills required:Clinical Research, Pharmacovigilance, Clinical Trials, Clinical Data Management and PharmacologyOther Requirements:B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, or related pharmaceutical/healthcare backgrounds.Freshers and students who are interested in Pharmacovigilance / Drug Safety can apply.Basic understanding of pharmacology, adverse drug reactions, and medicines is preferred.Good written and verbal communication skills.Good attention to detail and documentation skills.Basic computer and MS Office/Google Workspace knowledge.Ability to work independently in a Work From Home environment.Candidates should be able to commit to the complete 3-month internship.About Company:'The ARZON GLOBAL LABS - Built on Experience, Driven by Impact.'

ARZON was founded to address long-standing gaps in education, such as poor training quality, limited placement support, and a lack of trust. After mentoring over 100,000 learners, our team created a platform that prioritizes real-world outcomes and transparency. We deliver domain-specific programs, live sessions, hands-on projects, mentorship, and verified credentials via our Skills Wallet. With trust and innovation at our core, ARZON is here to empower careers and redefine how learning connects to opportunity.Additional information:

Stipend Structure:

Fixed pay: ₹ 5,000 - 10,000 /month

Incentive pay: ₹ 1,000 - 5,000 /month

Responsibilities

Selected intern's day-to-day responsibilities include:

Arzon Global is looking for motivated and detail-oriented Pharmacovigilance Interns to join our Drug Safety team. This internship provides practical exposure to pharmacovigilance, adverse drug reaction (ADR) reporting, safety data review, case processing, and drug-safety documentation.

The ideal candidate should have a basic understanding of medicines and pharmacology, strong attention to detail, good documentation skills, and an interest in pursuing a career in pharmacovigilance or the pharmaceutical industry.

1.Assist the pharmacovigilance team in reviewing and documenting Adverse Drug Reaction (ADR) information.

Support the identification and collection of relevant safety information from available sources.

Assist with Individual Case Safety Report (ICSR) data entry and case documentation under supervision.

Review case information for completeness, consistency, and accuracy.

2.Assist in identifying important patient, drug, and adverse-event information from case narratives.

Support the documentation and maintenance of pharmacovigilance records.

Assist with basic case follow-up activities and information tracking as assigned.

Support medical literature review activities related to drug safety, where applicable.

3.Assist in maintaining safety databases, spreadsheets, and relevant documentation.

Follow standard operating procedures (SOPs) and data-quality requirements.

Maintain confidentiality of patient and safety-related information.

Support the team in preparing reports, trackers, and other pharmacovigilance-related documentation.

Perform other drug-safety and pharmacovigilance activities assigned by the supervisor.