01Overview
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 prospect 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:
1. Internship Program
Role: Pharmacovigilnce intern(Paid Internship)
Duration: 3 months
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.
- Robust 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 .
