Are you a Pharmacy or Life Sciences graduate looking to enter the world of pharmacovigilance and drug safety? Here’s an exciting opportunity to gain hands-on industry exposure with a globally recognized organization — ProPharma.
If you’re trained in the Argus Safety Database and want real-world experience in case processing and regulatory reporting, this 12-month internship program in Hyderabad could be your ideal career launchpad 🚀.
🌍 About ProPharma
For over two decades, ProPharma has supported biotech, pharmaceutical, and medical device companies in bringing innovative therapies to patients safely and efficiently.
The company provides services across the entire product lifecycle, including:
- Regulatory Sciences
- Clinical Research
- Pharmacovigilance
- Quality & Compliance
- Medical Information
- R&D Technology Solutions
With a strong global presence, ProPharma follows an advise–build–operate model, helping clients accelerate drug development while maintaining compliance with international regulations.
🧪 Job Role: Pharmacovigilance Intern
📍 Location: Hyderabad (Work from Office)
⏳ Duration: 12 Months
🏢 Department: Pharmacovigilance
🕒 Employment Type: Full-Time Internship
This internship is specially designed for candidates with basic exposure to the Argus Safety Database who want to strengthen their practical skills in case processing and regulatory compliance.
📌 Key Responsibilities
📥 Mailbox Management & Triage
- Handling safety mailboxes
- Reviewing inbound adverse event reports
- Sorting client and internal communications
- Ensuring proper documentation for processing
🔎 Duplicate Search & Initial Book-In
- Performing duplicate searches within the safety database
- Completing initial case entry procedures
- Verifying essential reporting components
🗂 Data Entry in Safety Database
Entering critical case details such as:
- Identifiable patient information
- Reporter details
- Suspect drug
- Adverse events
Accuracy at this stage is crucial, as small errors can impact regulatory submissions.
🧾 Case Processing Support
- Assisting in Argus-based case handling
- Conducting follow-ups
- Ensuring reporting timelines are met
✍️ Narrative Writing & MedDRA Coding
- Supporting preparation of medical narratives
- Performing MedDRA coding
- Maintaining compliance with global regulatory standards
📊 ICSR Management
- Assisting with Individual Case Safety Reports (ICSRs)
- Supporting timely submissions to regulatory authorities
🤝 Cross-Functional Collaboration
- Coordinating with safety physicians and regulatory teams
- Following internal SOPs and pharmacovigilance guidelines
🎓 Eligibility Criteria
✔️ Completed degree in:
- B.Pharm / M.Pharm
- Pharm.D
- Life Sciences
- Medicine or related field
✔️ Basic knowledge or prior training in Argus Safety Database
✔️ Understanding of:
- Pharmacovigilance principles
- Drug safety regulations
- Adverse event reporting
✔️ Strong attention to detail
✔️ Good communication skills
✔️ Proficiency in Microsoft Office
💡 Why This Internship Is a Strong Career Move
🌟 Real-World Case Handling
Work on actual safety cases — not simulations.
📈 Industry-Relevant Skill Development
Gain expertise in:
- ICSR processing
- Narrative writing
- MedDRA coding
- Regulatory compliance
👩🏫 Mentorship from Experts
Learn directly from experienced drug safety professionals.
🌎 Global Exposure
Understand international pharmacovigilance standards in a consulting environment.
🚀 Career Progression Opportunities
This internship can lead to roles such as:
- Drug Safety Associate
- Pharmacovigilance Executive
- Safety Data Analyst
- Regulatory Affairs Associate
🧠 Skills You Will Develop
By the end of 12 months, you will strengthen:
- Analytical thinking
- Regulatory knowledge
- Database management skills
- Medical writing basics
- Time management
- Compliance awareness
These competencies are highly valued in pharmaceutical companies, CROs, and global safety centers.
📍 Why Hyderabad Is a Growing Pharmacovigilance Hub
Hyderabad has emerged as a major pharmaceutical and life sciences hub in India 🏙️. With numerous CROs, biotech firms, and pharma companies operating in the region, the city offers:
- Strong networking opportunities
- Exposure to multinational projects
- Structured corporate training environments
- Long-term career growth in drug safety
Working from the office ensures:
- Real-time mentorship
- Better team collaboration
- Strong professional discipline
📝 Who Should Apply?
This internship is ideal for:
- Fresh graduates with Argus training
- Candidates entering pharmacovigilance
- Pharmacy students seeking practical exposure
- Professionals building a long-term career in drug safety
If you are serious about entering pharmacovigilance, this role offers the right mix of learning, compliance exposure, and real case handling 📚.
👉 Apply here:
https://propharmagroup.wd1.myworkdayjobs.com/en-US/ppgcareers/job/Pharmacovigilance-Intern_JR7887
🔍 Final Thoughts
Breaking into pharmacovigilance can be challenging without hands-on experience. This 12-month Pharmacovigilance Internship at ProPharma provides structured exposure, regulatory insight, and professional growth within a global organization.
If you meet the eligibility criteria and are ready for a fast-paced, compliance-driven environment, this could be your gateway into the pharmaceutical industry.
Stay proactive. Keep upgrading your skills. Build your expertise step by step 💪
