Discover pharmacovigilance jobs at ProPharma! Apply now for this full-time role in India, driving safety in clinical research and regulatory compliance.
Contents
About the Company
ProPharma Group, with over 20 years of excellence, empowers biotech, medtech, and pharmaceutical innovators worldwide through its advise-build-operate model. As a leading global provider of regulatory, clinical, and compliance services, it supports the full product lifecycle with deep expertise in pharmacovigilance, quality assurance, and R&D technology.
Boasting 2,500+ professionals across GMP/GDP-compliant operations, ProPharma accelerates breakthroughs while ensuring regulatory adherence. Its commitment to diversity, equity, and inclusion fosters a collaborative environment, making it a top choice for pharmaceutical careers in India and beyond.
Job Details
- Company Name: ProPharma Group
- Experience: Preferred 1 year (entry-level considered)
- Qualification: Post-secondary education
- Location: India
- Work Type: Full-time
Job Description
ProPharma Group is seeking a dedicated Pharmacovigilance Coordinator to enhance its global safety monitoring efforts. This role supports biotech and pharma clients in managing adverse event reporting and compliance. Ideal for those passionate about pharmacovigilance jobs, it offers hands-on involvement in safety databases and client communications.
Pharmacovigilance Coordinator
- Department: Pharmacovigilance
- Role: Pharmacovigilance Coordinator
- Experience: Preferred 1 Year
- Education/Qualification: Post-secondary education
Skills/Qualifications
- Strong verbal, written, and interpersonal communication skills
- Proficient in computer operations and keyboarding
- Excellent organization, prioritization, and attention to detail
- Ability to work independently and collaboratively in teams
- Basic knowledge of pharmacovigilance processes and databases
- Familiarity with PHI redaction and regulatory triage preferred
Key Responsibilities
- Manage mailboxes and triage client/inbound reports
- Perform duplicate searches and initial case book-in
- Screen/redact source documents for PHI compliance
- Facilitate literature activities and database searches
- Send draft reports to clients for review
- Enter data into safety databases (patient, drug, events)
- Support full data entry post-training as needed
Benefits/Perks
- Career growth in a global pharmacovigilance leader
- Continuous learning through domain expertise programs
- Competitive salary and performance incentives
- Inclusive culture promoting diversity and authenticity
- Collaborative environment with work-life balance
- Global exposure to high-profile drug/device programs
How to Apply
Submit your application directly through ProPharma’s careers portal at ProPharma Careers. Include your resume and a cover letter highlighting pharmacovigilance interest. All applications receive personal review—no AI screening.
Verified Post
The post is released by the ProPharma Career page. Click here to visit the post
Note: ProPharma does not accept unsolicited resumes from recruiters. For more pharma jobs in India, check Pharma Recruiter. Elevate your career—apply today and contribute to patient safety innovations!
Why You Should Join
ProPharma Group champions a vibrant, equitable workplace where innovation meets impact, earning acclaim for empowering diverse teams to drive health advancements. With stable growth in regulatory and clinical spaces, it offers long-term security and skill enhancement in pharmacovigilance.
Join a culture that values authenticity, collaboration, and entrepreneurial spirit, accelerating your pharmaceutical careers in India while de-risking groundbreaking therapies for global patients.
FAQs
Who qualifies for this pharmacovigilance coordinator role?
Post-secondary graduates with preferred 1 year in industry; strong communication and organizational skills essential for entry into pharma jobs.
How does the application process work at ProPharma?
Applications are manually reviewed by recruiters for personalized feedback—expect a response regardless of outcome. No fees or third-party involvement.
What does a typical day involve in pharmacovigilance jobs here?
Triage emails, data entry into safety systems, document redaction, and client coordination to ensure timely adverse event reporting.
Are there advancement opportunities in clinical research or QA?
Yes, with training in regulatory sciences and global projects, fostering rapid growth in compliance and pharmacovigilance careers.