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Are you a 2025 pharmacy, medical, or life sciences graduate looking to start your career in pharmacovigilance and drug safety? This could be your perfect opportunity!
Syneos Health, a global biopharmaceutical solutions leader, is inviting fresh graduates to join as Safety & Pharmacovigilance Trainees in Gurugram. This role is designed for young professionals eager to gain hands-on exposure to case processing, safety databases, regulatory compliance, and global drug safety operations.
With more than 29,000 employees across 110 countries, Syneos Health provides a dynamic and inclusive work environment where every individual’s contribution matters. If you are passionate about healthcare innovation and want to build a career that directly impacts patients’ lives, this is the right place to begin.
📍 Location: Gurugram, India
🕒 Job Type: Full Time
🆔 Job ID: 25101070
📅 Posted On: Today
⏳ Last Date to Apply: August 23, 2025
About Syneos Health
Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization built to accelerate customer success. The company translates clinical, medical affairs, and commercial insights into meaningful outcomes that address today’s healthcare challenges.
At Syneos Health, work truly matters everywhere. The organization emphasizes career growth, diversity, inclusion, and its “Total Self” culture, ensuring employees feel supported both professionally and personally.
Role: Safety & Pharmacovigilance – Trainee
This entry-level position gives graduates a strong foundation in drug safety and pharmacovigilance operations. As a trainee, you will be responsible for supporting case management, safety reporting, and regulatory submissions, while learning from experienced professionals in a global setup.
Key Responsibilities
- Monitor and route incoming safety information.
- Record and track ICSR documentation per sponsor/customer specifications.
- Ensure patient confidentiality as per GCP/GVP guidelines.
- Enter cases into safety databases and maintain consistency.
- Support safety literature review, MedDRA coding, and narrative writing.
- Assist in submission processes, reconciliation activities, and audits.
- Maintain essential documentation for TMF and PSMF.
Eligibility & Qualifications
- Education:
- M.Pharm, Pharm.D, M.Sc + B.Pharm, BHMS, BDS, or Ph.D. (Pharmacy).
- Passout Year: 2025 (2024 passouts may also apply with strong interest in pharmacovigilance).
- Required Skills:
- Strong healthcare/scientific knowledge.
- Proficiency in MS Office Suite & Outlook.
- Excellent documentation and communication skills.
- Strong organizational and multitasking ability.
- Accuracy and attention to detail.
- Preferred:
- Familiarity with pharmacovigilance processes, safety databases, and medical terminology.
- Experience with collaboration tools like Visio or Team Share.
Additional Information
- This is a 1-year trainee role with possible extension based on performance and business needs.
- A great stepping stone for graduates aiming for a career in pharmacovigilance and clinical research.
🌐 Apply Now
If you meet the eligibility criteria and aspire to build your career in drug safety, apply online before August 23, 2025.
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