Safety & PV Coordinator Job at Syneos Health – Pharmacovigilance Role | Hyderabad | 0–3 Years

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Safety & PV Coordinator Job at Syneos Health | Pharmacovigilance | Hyderabad | 2026

Syneos Health
Hyderabad
0–3 Years
Pharmacovigilance
PV Submissions
Office-Based

📄 About the Company

Syneos Health® is a fully integrated biopharmaceutical solutions organization operating in 110+ countries with over 29,000 employees worldwide.

The company partners with pharmaceutical and biotech clients to accelerate drug development, improve patient outcomes, and support clinical and commercial success across the product lifecycle.

📌 Job Overview

Syneos Health is hiring a Safety & Pharmacovigilance (PV) Coordinator for its Hyderabad office.

This is a full-time, office-based role ideal for candidates with 0–3 years of experience in pharmacovigilance submissions, safety reporting, or clinical research operations.

The role focuses on PV submission coordination, safety documentation, and regulatory compliance in a global environment.

🧪 Job Details – Safety & PV Coordinator

Company: Syneos Health

Position: Safety & PV Coordinator

Location: Hyderabad, India

Experience Required: 0–3 Years

Work Mode: Office-Based (Onsite)

Employment Type: Full-Time

Domain: Pharmacovigilance / Drug Safety / PV Submissions

🧾 Key Responsibilities

  • Maintain tracking and documentation of safety submissions
  • Build professional relationships with internal and external project teams
  • Apply safety reporting regulatory intelligence across assigned activities
  • File and manage project documents (electronic and hardcopy)
  • Support design, preparation, and assembly of expedited and periodic safety reports
  • Assist with miscellaneous tasks related to safety reporting and compliance
  • Forward completed safety documents to clients and stakeholders
  • Ensure compliance with SOPs, Work Instructions (WIs), GCP, ICH, and global safety regulations

🎓 Required Qualifications

  • B.Pharm / M.Pharm / Pharm.D
  • BSc / MSc – Life Sciences
  • Nursing / Biotechnology or related discipline
  • Experience in pharmacovigilance submission or safety reporting preferred
  • Clinical research experience is an added advantage

🧠 Required Skills

  • Good understanding of global pharmacovigilance regulations
  • Strong documentation and coordination skills
  • Excellent verbal and written communication
  • Ability to work in a fast-paced, process-driven environment
  • Proficiency in MS Office and safety tracking systems
  • Strong organizational and time management skills

💼 Why Work at Syneos Health?

  • Exposure to global cross-functional pharmacovigilance teams
  • Structured career development and growth pathways
  • Inclusive “Total Self” work culture
  • Competitive compensation and global recognition programs
  • Opportunity to work with leaders shaping future healthcare innovations

💰 Salary Range (Estimated)

  • ₹4.5 LPA – ₹7.5 LPA
  • Salary may vary based on experience, skills, and interview performance
📌 Note Before You Apply:
We use a 15-second timer to encourage candidates to read the job description carefully before applying. Please ensure your experience aligns with PV submission and safety coordination responsibilities.

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