Pharmacovigilance Jobs at Syneos Health | BSc Life Science Candidates Apply Now
Are you looking for a rewarding career in pharmacovigilance and clinical safety? Syneos Health is hiring a Safety & PV Coordinator in Gurgaon, Haryana, India. Join a leading biopharmaceutical solutions organization where your work impacts patient safety, accelerates therapy delivery, and contributes to global healthcare advancements.
About the Company
Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization designed to accelerate customer success. By translating unique clinical, medical affairs, and commercial insights into outcomes, Syneos Health addresses modern market realities. With a Clinical Development model centered on both the customer and the patient, the company continuously simplifies and streamlines work processes to enhance both client and employee experiences.
Job Details
Job Post: Safety & PV Coordinator
Qualifications and Skills:
- Bachelor’s Degree in life sciences, nursing, pharmacy, or equivalent experience
- Familiarity with safety database systems and medical terminology preferred
- Proficiency in Microsoft Office Suite, email, TeamShare, and the internet
- Strong organizational, documentation, and communication skills
- Detail-oriented with the ability to prioritize multiple tasks
- Team player with a professional work ethic
Why Work at Syneos Health:
- Career development and progression opportunities
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition and total rewards programs
- Inclusive Total Self culture fostering authenticity and belonging
Job Responsibilities – Safety & PV Coordinator:
- Monitor and route incoming information to relevant projects
- Record ICSR documentation per sponsor/customer specifications
- Redact patient-identifying information following data protection and regulatory guidelines
- Enter data into the safety database following standard operating procedures
- File creation, tracking, retention, and maintenance (paper and electronic)
- Manage translations of source documents, query follow-ups, and submission processes
- Assist with literature screening, narrative writing, coding of events, medications, and tests
- Validate xEVMPD product records and manually recode unrecoded terms if required
- Identify and manage duplicate ICSRs and activities related to SPOR / IDMP
- Ensure submission of relevant documents to the Trial Master File (TMF)
- Maintain understanding of SOPs, global regulations, GCP, ICH guidelines, GVP modules, and study plans
- Participate in audits and foster professional relationships with team members
About Syneos Health Achievements:
- Supported 94% of all Novel FDA-approved drugs and 95% of EMA Authorized Products in the past five years
- Managed over 200 studies across 73,000 sites and 675,000+ trial patients
- Encourages employees to take initiative and challenge the status quo in a dynamic environment
Note:
This posting is for a potential upcoming opportunity. By expressing interest, candidates are added to Syneos Health’s talent pipeline for consideration when the role becomes available.
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