Pharmacovigilance Intern Job Opening at ProPharma, Hyderabad
| Pharmacovigilance Intern Job in Hyderabad - Apply Now |
About ProPharma
For over 20 years, ProPharma has empowered biotech, med device, and pharmaceutical companies to advance scientific breakthroughs. Offering end-to-end consulting in regulatory sciences, clinical research, pharmacovigilance, medical information, and R&D technology, ProPharma helps clients de-risk and accelerate high-profile drug and device programs.
Job Location & Duration
Location: Hyderabad, India (Work from Office)
Duration: 12 Months
Department: Pharmacovigilance
Role Overview
The Pharmacovigilance Intern role offers hands-on exposure to drug safety processes, case management, and regulatory reporting. Interns will gain experience working with the Argus safety database and other pharmacovigilance tools while supporting cross-functional teams.
Key Responsibilities
Manage assigned mailboxes: triage client communications, inbound reports, and internal case processing messages.
- Perform duplicate searches and complete initial book-in.
- Enter data into the safety database: patient information, report details, suspect drug, and adverse event.
- Assist in case processing within the Argus database, including follow-ups.
- Support narrative writing and MedDRA coding.
- Assist in Individual Case Safety Report (ICSR) management per regulatory standards.
- Collaborate with cross-functional teams to ensure timely adverse event reporting.
- Maintain accurate documentation and adhere to pharmacovigilance compliance standards.
Requirements
- Degree in Pharmacy, Life Sciences, Medicine, or related field.
- Basic knowledge or prior training in Argus safety database.
- Understanding of pharmacovigilance principles and drug safety regulations.
- Strong attention to detail, analytical skills, and ability to work in fast-paced environments.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Excellent verbal, written, and interpersonal communication skills.
What ProPharma Offers
- Hands-on experience in global pharmacovigilance.
- Exposure to real-world case processing and regulatory compliance.
- Mentorship from industry experts.
- Career enhancement opportunities in drug safety and regulatory affairs.
- Inclusive, diverse, and collaborative work environment
How To Apply: 👉Click Here For Apply
Frequently Asked Questions (FAQs)
Q1: What is the eligibility for the Pharmacovigilance Intern role?
A: Candidates should have a degree in Pharmacy, Life Sciences, Medicine, or a related field with basic knowledge of Argus.
Q2: Where is the internship located?
A: The internship is in Hyderabad, India (Work from Office).
Q3: How long is the internship duration?
A: The internship lasts 12 months.
Q4: Will I get hands-on experience?
A: Yes, interns gain practical experience in case processing, regulatory reporting, and pharmacovigilance workflows.
Q5: Do I need prior experience with Argus?
A: Basic knowledge or prior training in Argus safety database is required.
Q6: What career opportunities are available after this internship?
A: Interns may advance in pharmacovigilance, regulatory affairs, and global drug safety roles.
Q7: Is this internship full-time?
A: Yes, this is a full-time internship.
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