Syneos Health Pharmacovigilance Job Opening | Safety & Pharmacovigilance Coordinator | Pharma Job
Looking for a Pharmacovigilance job in the global pharmaceutical industry? Syneos Health is hiring a Safety & Pharmacovigilance Coordinator, offering a great Pharma job opportunity for candidates with experience in clinical trial or literature data entry. This Pharmacovigilance job allows professionals to work with a leading biopharmaceutical solutions organization that focuses on drug safety monitoring, regulatory compliance, and case processing in global clinical programs. If you are seeking a rewarding Pharma job in drug safety and pharmacovigilance, this opportunity could be a strong step in your career.
- Position: Safety & Pharmacovigilance Coordinator
- Location: Gurgaon, Haryana
About the Company
Syneos Health is a leading, fully integrated biopharmaceutical solutions organization built to accelerate customer success. The company translates unique clinical, medical affairs, and commercial insights into outcomes that address modern market realities.
Syneos Health’s Clinical Development model brings the customer and the patient to the center of everything they do. The organization continuously looks for ways to simplify and streamline its work to make Syneos Health easier to work with and easier to work for.
Job Description
The Pharmacovigilance job involves working closely with project teams to monitor safety information, perform accurate data entry into safety databases, and support pharmacovigilance activities related to clinical trials and literature case processing in the pharmaceutical industry.
Key Responsibilities
- Monitor incoming safety reports and forward them to the correct project teams.
- Record and track ICSR (Individual Case Safety Reports) as per sponsor guidelines.
- Remove patient-identifying information from documents to comply with data protection and ICH-GCP / GVP requirements.
- Enter safety data accurately into the safety database within required timelines.
- Help create, organize, and maintain case files (both electronic and paper).
- Support translation of source documents when required.
- Assist with follow-up queries related to safety cases.
- Support safety submission activities when instructed.
- Help reconcile daily workflow and case processing activities.
- Maintain knowledge of SOPs, work instructions, GCP, ICH guidelines, and drug safety regulations.
Qualifications
- Healthcare professional by education: B.Pharm / M.Pharm / PharmD.
- Minimum 1 year of experience in Pharmacovigilance in a full data entry or case processing role is mandatory.
- Experience in processing Literature and Clinical Trial (CT) cases is preferred.
- Experience with safety database systems and medical terminology preferred.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), Visio, Outlook, TeamShare (or similar document management systems), and internet applications.
- Strong ability to work collaboratively as part of a team.
- Ability to prioritize and manage multiple tasks effectively in a fast-paced environment.
- Excellent written and verbal communication and interpersonal skills.
- Strong organizational and documentation skills with high attention to detail and accuracy.
- Should be flexible to work in rotational shifts.
