Job Title: Safety & Pharmacovigilance - Trainee (Contractual | 2025 Passout Only)
Location: Gurugram, India
Job ID: 25101070
About the Company:
Syneos Health® is a leading integrated biopharmaceutical solutions organization dedicated to accelerating customer success. With 29,000 employees across 110 countries, the company works with 94% of all novel FDA-approved drugs and 95% of EMA-authorized products, focusing on innovation, patient-centric approaches, and career development opportunities.
Role Overview:
The Safety & Pharmacovigilance Trainee will support departmental and project deliverables related to the preparation and processing of Individual Case Safety Reports (ICSRs), literature screening, drug coding, MedDRA coding, safety database entry, and global pharmacovigilance compliance. This is a contractual role for 1 year, extendable based on performance and business needs.
Key Responsibilities:
Monitor and route incoming safety information to appropriate projects.
Record and track ICSR documentation in line with sponsor/customer specifications.
Redact patient-identifying information per data protection guidelines, ICH-GCP, and GVP.
Assist with safety database entry and ensure adherence to conventions.
Manage file creation, retention, and maintenance (electronic/paper).
Support translation, query follow-up, and submission processes.
Contribute to literature screening, drug dictionary maintenance, MedDRA coding, and narrative writing.
Validate xEVMPD product records, manage duplicate ICSRs, and handle SPOR/IDMP activities.
Ensure compliance with SOPs, WIs, global regulations, and pharmacovigilance guidelines.
Participate in audits and foster professional collaboration with team members.
Required Qualifications:
Education: M.Pharm, Pharm.D, M.Sc + B.Pharm, BHMS, BDS, or Ph.D. (Pharmacy).
Eligibility: 2025 graduates. Exceptional 2024 graduates with a strong interest in pharmacovigilance may also apply.
Strong scientific/healthcare knowledge.
Proficiency in Microsoft Office Suite and Outlook.
Excellent written and verbal communication skills.
Strong organizational, documentation, and multitasking skills.
High attention to detail and accuracy.
Preferred Qualifications:
Familiarity with pharmacovigilance, medical terminology, safety databases, and drug coding.
Experience with collaboration tools such as Visio or Team Share.
Important Note:
This is a contractual trainee position for one year, subject to renewal based on performance and business requirements. Comprehensive pharmacovigilance training will be provided before transition into project roles.
Estimated Salary: ₹3.2 – 4.5 LPA (based on industry standards for trainee pharmacovigilance roles in Gurugram).
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Tallinn |Hà Nội :
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Japan | Saitama |Tokyo :
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Kyiv |Lima Region :
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