ARZON GLOBAL LABS is looking for enthusiastic, detail-oriented, and motivated candidates to join our Pharmacovigilance and Clinical Trials & Clinical Research Internship Program.

This internship provides hands-on exposure to drug safety monitoring, adverse event reporting, clinical trial processes, clinical research documentation, data management, and regulatory requirements. It is an excellent opportunity for candidates aspiring to build a career in Pharmacovigilance, Clinical Research, Clinical Trials, Drug Safety, and Regulatory Affairs.

Internship Details

Role: Pharmacovigilance & Clinical Trials/Clinical Research Intern
Duration: 3 Months
Internship Type: Paid Internship
Location: Madhapur, Hyderabad / Remote
Stipend: 10,000 per month

Key Responsibilities

- Assist in monitoring and evaluating Adverse Drug Reactions (ADRs) and other drug safety information.
- Support the collection, review, and processing of safety data from various sources.
- Assist in Individual Case Safety Report (ICSR) processing and safety documentation.
- Support clinical trial documentation and study-related activities.
- Assist in the preparation, review, and maintenance of essential clinical trial documents.
- Collect, organize, and maintain clinical research and safety data.
- Support clinical trial coordination, study activities, timelines, and documentation.
- Assist with data entry, data verification, and quality checks.
- Maintain accurate records, databases, trackers, and research-related documentation.
- Assist in preparing study reports and other clinical research documents.
- Develop an understanding of clinical trial protocols, research procedures, and pharmacovigilance workflows.
- Support signal detection and risk assessment activities.




- Assist in ensuring compliance with applicable pharmacovigilance and clinical research guidelines and regulatory requirements.
- Coordinate with internal teams for data management, documentation, and reporting.

Eligibility Criteria

- Only Freshers and Currently Pursuing Candidates Can Apply.
- Candidates who are currently pursuing graduation or post-graduation are eligible.
- Fresh graduates with no prior work experience are encouraged to apply.
- Candidates with previous work experience are not eligible for this internship.
- B.Pharm, M.Pharm, Pharm.D, D.Pharm, Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, or related fields.
- Basic understanding of Pharmacovigilance, Clinical Research, or Clinical Trials is preferred.
- Positive communication and documentation skills.
- Strong analytical thinking and attention to detail.
- Basic knowledge of MS Office.

Required Skills

- Attention to Detail
- Analytical Thinking
- Communication Skills
- Documentation & Reporting
- Clinical Documentation
- Data Management
- Research Skills
- Basic Computer Knowledge
- Team Collaboration
- Time Management
- Problem-Solving Skills

Learning & Growth Opportunities

- Hands-on exposure to Pharmacovigilance, Drug Safety, Clinical Trials, and Clinical Research processes.
- Practical understanding of ADR reporting and ICSR case processing.
- Exposure to clinical trial documentation, study workflows, and clinical research procedures.
- Understanding of clinical data management and study coordination.
- Exposure to regulatory guidelines and compliance requirements.
- Development of analytical, documentation, communication, and research skills.
- Internship Completion Certificate.
- Industry exposure with potential career opportunities in Pharmacovigilance, Clinical Research, Clinical Trials, Drug Safety, and Regulatory Affairs.

📌 Pharmacovigilance Intern and clinical trials & research (Hyderabad)
🏢 Arzon Global
📍 Hyderabad