Pharmacovigilance Internship at Syneos Health Careers | Safety & PV Intern | Apply Now
Looking to begin your career in Drug Safety and Pharmacovigilance? This latest Pharmacovigilance Internship opportunity at Syneos Health Careers is ideal for freshers seeking hands-on exposure in safety database management, MedDRA coding, ICSR processing, and global pharmacovigilance operations. The Safety & PV Intern/Trainee role in Hyderabad offers excellent learning opportunities for Pharmacy graduates interested in building a career in clinical research and drug safety.
- Position: Safety & PV Intern/Trainee
- Location: Hyderabad
About the Company
Syneos Health is a leading, fully integrated life sciences services organization focused on accelerating customer success across the drug development and commercialization continuum. Through innovative clinical solutions and healthcare expertise, Syneos Health supports pharmaceutical and biotechnology companies globally.
At Syneos Health Careers, employees gain exposure to advanced clinical research, pharmacovigilance, and regulatory processes while working in a collaborative and inclusive environment.
Job Description
Syneos Health is hiring for the position of Safety & PV Intern/Trainee at its Hyderabad office. This Pharmacovigilance Internship is designed for fresh graduates and candidates passionate about drug safety, pharmacovigilance operations, MedDRA coding, ICSR management, and regulatory compliance.
The role provides hands-on exposure to safety reporting activities, literature screening, database management, and global pharmacovigilance practices aligned with ICH GCP and GVP guidelines.
Key Responsibilities
- Monitors and routes incoming information to the appropriate project.
- Records and tracks ICSR documentation according to Sponsor/customer specifications.
- Redacts patient-identifying information/images in accordance with data protection and GVP guidelines.
- Assists with safety database case creation and data entry.
- Ensures proper conventions are followed while entering cases into safety databases.
- Supports file tracking, retention, and maintenance activities.
- Assists with translation processes for source documents.
- Supports query follow-up and submission processes.
- Assists with workflow reconciliation activities.
- Performs literature screening and review for safety information.
- Supports MedDRA coding and drug coding activities.
- Assists with narrative writing and event coding.
- Supports expedited safety reporting activities.
- Assists with xEVMPD product record validation.
- Supports duplicate ICSR identification and management.
- Participates in SPOR/IDMP-related activities.
- Maintains TMF and Pharmacovigilance System Master File documentation.
- Participates in audits and safety reporting compliance activities.
Qualifications
Educational Qualification
- M.Pharm
- Pharm.D
- B.Pharm
- Ph.D. (Pharmacy)
Eligibility Criteria
- 2025 pass-out candidates are eligible.
- 2024 pass-out candidates with a strong interest in Pharmacovigilance may also apply.
Core Skills Required
- Strong healthcare/scientific background knowledge.
- Interest in Drug Safety and Pharmacovigilance.
- Proficiency in Microsoft Office Suite and Outlook.
- Excellent documentation and organizational skills.
- Strong written and verbal communication abilities.
- Ability to work collaboratively in teams.
- close attention to detail and accuracy.
