Pharmacovigilance Internship – Hyderabad
Summary: ProPharma is seeking a highly motivated and detail-oriented Pharmacovigilance Intern to join our dynamic team in Hyderabad. This 12-month, work-from-office internship offers invaluable hands-on experience in drug safety, case management, and Argus safety database operations. If you’re a recent graduate with a passion for pharmacovigilance and a desire to contribute to global patient safety, we encourage you to apply!
About ProPharma:
ProPharma is a global leader in providing regulatory science and drug safety solutions to the pharmaceutical, biotechnology, and medical device industries. We are committed to helping our clients bring innovative therapies to market safely and efficiently. Our team is comprised of dedicated professionals who are passionate about making a difference in the lives of patients around the world.
Job Description:
We are currently seeking a Pharmacovigilance Intern to support our drug safety team in Hyderabad. This internship provides an excellent opportunity to gain practical experience in various aspects of pharmacovigilance, including case processing, adverse event reporting, and database management. As a Pharmacovigilance Intern, you will work alongside experienced professionals and contribute to the safety monitoring of pharmaceutical products.
Key Responsibilities:
- Manage pharmacovigilance mailboxes, including triaging client communication and safety reports, ensuring timely and accurate responses.
- Conduct duplicate searches within the safety database to identify potential duplicate case reports.
- Perform initial case intake, including verifying information and logging cases into the tracking system.
- Enter key case details, such as patient demographics, drug information, and adverse events, into the Argus safety database.
- Assist with case processing activities, including preparing case narratives and performing MedDRA coding of adverse events.
- Support Individual Case Safety Report (ICSR) management to ensure compliance with global regulatory timelines and requirements.
- Collaborate effectively with cross-functional teams, including medical affairs, regulatory affairs, and clinical development, to ensure timely and accurate adverse event reporting.
- Maintain compliance with established pharmacovigilance standards, Standard Operating Procedures (SOPs), and documentation protocols.
- Participate in training sessions and workshops to enhance knowledge and skills in pharmacovigilance and drug safety.
- Assist with other pharmacovigilance-related tasks as assigned by the supervisor.
Qualifications Required:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Medicine, or a related field.
- Basic knowledge and prior experience/training with Argus safety database is preferred.
- Understanding of pharmacovigilance principles and drug safety compliance regulations.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) is essential.
- Excellent written and verbal communication skills in English.
- Strong attention to detail and ability to maintain accuracy in a fast-paced environment.
- Ability to work independently and as part of a team.
- Strong organizational and time management skills.
- A proactive and enthusiastic attitude with a willingness to learn.
Benefits of Joining ProPharma:
- Practical training in global pharmacovigilance case processing and regulatory requirements.
- Hands-on experience with real-world ICSR handling and adverse event reporting.
- Mentorship and guidance from experienced pharmacovigilance professionals.
- Opportunity to build a strong foundation for a career in drug safety and regulatory affairs.
- Exposure to a global pharmaceutical environment and cross-functional collaboration.
- Inclusive and diverse workplace that fosters innovation and growth.
- Valuable networking opportunities within the pharmaceutical industry.
This is a paid internship.
Location: Hyderabad, India
Duration: 12 Months
How to Apply:
If you are interested in this exciting opportunity to launch your career in pharmacovigilance, we encourage you to apply. Please submit your resume and cover letter through our online application portal. We look forward to hearing from you!