ProPharma is hiring for Pharmacovigilance Specialist, Submissions role in India. This full-time position offers a great opportunity for life sciences graduates seeking pharma jobs in drug safety and regulatory reporting. Explore this pharmaceutical career in a global PV environment.
Contents
- 1 About the Company
- 2 Job Details
- 3 Job Description
- 4 Skills/Qualifications
- 5 Key Responsibilities
- 6 Benefits/Perks
- 7 How to Apply
- 8 Why You Should Join
- 9 FAQs
- 9.1 What is the minimum qualification for the ProPharma Pharmacovigilance Specialist role?
- 9.2 Is prior experience mandatory for this pharma job?
- 9.3 What is the work model for this position in India?
- 9.4 How can I apply for this pharmacovigilance job?
- 9.5 Does ProPharma offer growth opportunities in PV submissions?
About the Company
ProPharma is a leading global provider of regulatory sciences, clinical research, quality & compliance, pharmacovigilance, medical information, and R&D technology solutions. With over 20 years of experience, the company partners with biotech, med device, and pharmaceutical organizations through an advise-build-operate model across the complete product lifecycle.
ProPharma helps clients de-risk and accelerate high-profile drug and device programs while maintaining the highest standards of patient safety and regulatory compliance. The firm continues to expand its presence in India, including a new office in Hyderabad, offering professionals strong growth in pharmacovigilance services.
Job Details
- Company Name: ProPharma
- Experience: 0-3 Years Exp
- Qualification: Post-secondary education or equivalent (life science degree preferred – B.Pharm, M.Pharm, Pharm.D, BSc, MSc)
- Location: India (Hybrid model encouraged for those near offices)
- Work Type: Full time
Job Description
ProPharma is actively hiring for the Pharmacovigilance Specialist, Submissions position in India. This role focuses on ensuring timely and compliant adverse event submissions within a multi-tenant Argus database environment.
It supports regulatory reporting to health authorities, ethics committees, and safety partners while contributing to periodic safety reports and system testing projects.
The position plays a critical part in maintaining pharmacovigilance compliance and operational excellence in a dynamic, multi-client setup.
Pharmacovigilance Specialist, Submissions
- Department: Pharmacovigilance
- Market: India
- Role: Pharmacovigilance Specialist, Submissions
- Experience: Proven experience preferred
- Education/Qualification: Post-secondary education (life science degree preferred)
Skills/Qualifications
- Post-secondary education or equivalent professional experience (life science degree preferred)
- Fluent in English
- Proven experience in a similar pharmacovigilance role highly preferred
- Proficient in Microsoft Office Suite (Outlook, Word, Excel) and strong keyboarding skills
- Excellent attention to detail
- Strong verbal, written, and interpersonal communication skills
- Flexibility to adapt to fluctuating business priorities
- Ability to work independently as well as collaboratively in a multidisciplinary team
Key Responsibilities
- Monitor daily scheduled ICSR submissions and safety partner exchanges
- Execute monthly ICSR reconciliation reports with clients and partners
- Assist in gateway-to-gateway submission testing and partner exchanges
- Generate Argus-based line listings and summary tabulations for periodic safety reports
- Support setup and verification of periodic safety report requirements
- Perform tester role in PQ testing for Argus upgrades, patches, and data migrations
- Create and close submissions-related deviations and CAPAs
- Update processes for new territory-specific E2B profiles
Benefits/Perks
- Career growth in a fast-expanding global pharmacovigilance organization
- Opportunities to work with advanced Argus systems and international clients
- Collaborative work culture that values diversity, equity, and inclusion
- Exposure to end-to-end product lifecycle projects
- Hybrid working model with support for in-office collaboration
- Professional development in regulatory compliance and drug safety
How to Apply
All applications to ProPharma roles are personally reviewed by the recruitment team. Apply directly through the official ProPharma careers portal using job requisition id JR 8766.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the ProPharma Career page.
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Visit the careers page here: ProPharma Careers. For more pharma jobs and pharmaceutical careers in India, explore listings on Pharma Recruiter.
Act now — submit your application today and take the next step in your pharmacovigilance career. You will receive an outcome on your application.
Why You Should Join
Joining ProPharma means becoming part of a mission-driven team committed to improving patient health and safety worldwide. The company fosters an innovative, inclusive culture where employees can unleash their entrepreneurial spirit while working on meaningful compliance and safety projects.
With a strong focus on long-term career stability, continuous learning, and global exposure, ProPharma provides an ideal environment for professionals seeking growth in regulatory sciences and pharmacovigilance.
Experience a supportive workplace that values authenticity, collaboration, and excellence in every submission and report.
FAQs
What is the minimum qualification for the ProPharma Pharmacovigilance Specialist role?
Post-secondary education with a life science degree (B.Pharm, M.Pharm, Pharm.D, BSc, MSc) preferred. Fluent English is required.
Is prior experience mandatory for this pharma job?
Proven experience in a similar role is highly preferred, but candidates with strong relevant skills may be considered.
What is the work model for this position in India?
Full-time role with a hybrid model encouraged for candidates near ProPharma offices.
How can I apply for this pharmacovigilance job?
Apply online via the official ProPharma Workday careers portal with requisition JR 8766. Unsolicited resumes from third parties are not accepted.
Does ProPharma offer growth opportunities in PV submissions?
Yes, the role provides exposure to Argus upgrades, new territories, periodic reports, and global compliance projects, supporting long-term career advancement in pharmaceutical careers.
