Pharmacovigilance Intern(Only Freshers)

Arzon Global Labs is looking for enthusiastic and detail-oriented freshers to join our Pharmacovigilance team. This internship provides hands-on exposure to drug safety monitoring, adverse event reporting, and regulatory compliance within the pharmaceutical industry. It is an excellent opportunity for candidates aspiring to build a career in Pharmacovigilance, Clinical Research, and Drug Safety. Please find the job description attached for your reference. Below are a few key details: Internship Program Role: Pharmacovigilnce intern (Only Fresher) Duration: 3 months(Paid Internship) Location: Madhapur, Hyderabad(Remote) Stipend: 10,000 Key Responsibilities Monitor and evaluate Adverse Drug Reactions (ADRs) and other drug safety information. Collect, review, and process safety data from various sources. Assist in Individual Case Safety Report (ICSR) processing and safety documentation. Maintain accurate records of pharmacovigilance activities and databases. Support signal detection and risk assessment activities. Ensure compliance with pharmacovigilance regulations and reporting timelines. Coordinate with internal teams for safety data management and reporting. Prepare and maintain accurate documentation related to drug safety activities. Eligibility Criteria B.Pharm, M.Pharm, Pharm.D, D.Pharm, or Life Sciences graduates. Freshers are encouraged to apply. Basic understanding of Pharmacovigilance and Clinical Research is preferred. Good communication and documentation skills. Strong analytical thinking and attention to detail. Basic knowledge of MS Office. Learning & Growth Opportunities Hands-on exposure to Pharmacovigilance workflows and drug safety operations. Practical knowledge of ADR reporting and ICSR case processing. Understanding of global regulatory guidelines and compliance requirements. Opportunity to develop analytical, documentation, and communication skills. Internship Completion Certificate. Industry exposure with potential career opportunities in Pharmacovigilance, Clinical Research, Drug Safety, and Regulatory Affairs. Required Skills Attention to Detail Analytical Thinking Communication Skills Documentation & Reporting Basic Computer Knowledge Team Collaboration Time Management Problem-Solving Skills Thank you for your consideration .