ProPharma Hiring Senior Pharmacovigilance Specialist: Hyderabad
Are you seeking rewarding safety analyst jobs via ProPharma Careers India or Senior Pharmacovigilance Specialist Jobs? Global clinical research, regulatory, and drug safety leader ProPharma is inviting applications for the position of Senior Pharmacovigilance Specialist at its India office (based in Hyderabad).
This role is ideal for experienced drug safety operations specialists with hands-on exposure to safety databases (Argus Safety or ARISg) and ICSR case processing. To prepare a compliance-focused resume for screening, read our detailed guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | ProPharma (PPG IN ProPharma Group India Pvt Ltd) |
| Job Title | Senior Pharmacovigilance Specialist |
| Job Location | Hyderabad, India (Hybrid Remote Options) |
| Employment Type | Full-Time |
| Experience Required | Minimum 3 Years in Pharmacovigilance |
| Qualifications | Bachelor's Degree in Life Sciences (Preferred: PharmD, RN, RPh, or Advanced Degree) |
| Department | Pharmacovigilance Case Processing |
| Job ID | JR 9902 |
💼 Key Responsibilities
- Responsible for overseeing and performing daily case processing of adverse event cases (both clinical trial and post-marketed safety cases).
- Perform precise coding using MedDRA terminology and determine seriousness and expectedness at event and case levels.
- Perform case follow-up activities, identifying critical clinical information required for submission.
- Write, review, and finalize high-quality safety case narratives.
- Provide timely client notifications as required for safety case management workflows.
- Highlight data discrepancies and workflow concerns to the Principal PV Specialist or Case Processing Manager.
- Maintain an up-to-date, operational knowledge of global regulatory guidelines and compliance rules.
- Perform thorough peer review of safety cases to ensure high quality, consistency, and accuracy.
- Perform Healthcare Professional (HCP) review of safety cases as needed.
- Mentor, train, and guide junior drug safety professionals within the project team.
To understand how senior safety specialist salaries scale between India, Europe, and America, read our analytical report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
Required Qualifications:
- Education: Bachelor's degree in Life Sciences (Pharmacy, Biotechnology, Biomedical Sciences, or related fields).
- Advanced Background: Advanced clinical degree (PharmD, RPh, Registered Nurse (RN), or equivalent) is highly preferred.
- Experience: Three (3) years of related work experience in a pharmacovigilance or drug safety database setup.
Technical & Professional Skills:
- Intermediate knowledge of pharmacovigilance principles and regulatory compliance.
- Working knowledge of safety databases, including Oracle Argus Safety, ARISg, or equivalent tools.
- Strong verbal, written, and interpersonal communication skills (essential for narrative writing).
- Intermediate project management skills and ability to identify and resolve problems.
- High level of accuracy, attention to detail, and ability to multitask effectively.
For life sciences professionals comparing corporate drug safety tracks with academic or regulatory clinical roles, read our guide on B.Pharm Careers after Graduation: India vs USA.
🎁 Program Benefits & Work Environment
- Direct exposure to global pharmacovigilance workflows and international client portfolios.
- Highly collaborative environment with modern, digital workflow management tools.
- Hybrid work model supporting remote work flexibility for candidates within commuting distance of the Hyderabad office.
- Structured learning paths and career growth opportunities inside a dedicated, global advisory group.
To test and improve your clinical trial compliance, safety definitions, and protocol coding knowledge, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Pharmacovigilance Operations vs Healthcare IT
Drug safety specialists monitor post-market adverse events, whereas healthcare IT professionals support electronic systems and EHR setups. To evaluate these career tracks, read our comparison on Healthcare IT vs Clinical Healthcare.
🚀 How to Apply?
Interested candidates should apply online directly on the official ProPharma Workday career portal. Click the button below to submit your resume:
Apply Online - ProPharma Workday Portal❓ Frequently Asked Questions
Q. What is the minimum experience required?
ProPharma requires candidates to have a minimum of 3 years of related work experience in a pharmacovigilance setup.
Q. Which degrees are preferred?
A Bachelor's degree in Life Sciences is required. Advanced degrees such as Pharm.D, RPh, or Registered Nurse (RN) credentials are highly preferred.
Q. Where will this role be based?
The role is located in Hyderabad, India, and supports hybrid remote work options.
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