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Hiring Central Monitor & Regulatory Affairs
🏢 Syneos Health
📍 Hyderabad / Gurugram / Mumbai
⏳ 1–3+ Years
💊 Clinical Research / Regulatory
Syneos Health is hiring for Central Monitoring and Regulatory Affairs roles across India. This is a strong opportunity for professionals looking to grow in clinical trials, risk-based monitoring, and regulatory submissions.
🧪 Central Monitor II / Senior Central Monitor
- Location: Hyderabad / Gurugram (Office-based)
- Experience: 2+ years (CM II) / 3+ years (Senior)
- Centralized monitoring & risk-based review
- Analyze patient data & dashboards
- Identify protocol deviations & safety signals
- Work with EDC, CTMS systems
- Ensure ICH-GCP compliance
📄 Regulatory Affairs Associate
- Location: Mumbai (Hybrid)
- Experience: 1–3 years (India Market)
- Drug registration & dossier submissions
- SUGAM portal & regulatory approvals
- Handle variations & import licenses
- Maintain regulatory documentation
- Support labeling & lifecycle updates
🎓 Eligibility
- B.Pharm / M.Pharm / PharmD / Life Sciences
- Experience in Clinical Monitoring or Regulatory Affairs
- Knowledge of ICH-GCP & regulatory guidelines
💻 Required Skills
- EDC / CTMS / Medidata Rave
- Data analysis & monitoring
- MS Excel & reporting
- SUGAM portal (for RA role)
💰 Salary
- Central Monitor: ₹6 – ₹14 LPA
- Regulatory Affairs: ₹4 – ₹9 LPA
🚀 Career Growth
- Clinical Operations / CRA
- Regulatory Affairs Specialist
- Clinical Data vs SAS Guide
💡 Interview Tips
- Revise ICH-GCP & RBM concepts
- Understand regulatory submissions
- PV Practice
📌 Tip: Apply to both roles if eligible to maximize chances.
🚀 Job Application Links (Syneos Health)
🚀 Apply Now: Central Monitor II / Sr. Central Monitor (Hyderabad / Gurugram)
🚀 Apply Now: Regulatory Affairs Associate (Mumbai)
📌 Important Note Before You Apply:
Kindly read the full job description carefully for your selected role before applying. Ensure your qualifications and profile align with centralized clinical trial data monitoring, risk indicators analysis, regulatory dossier compilation, lifecycle submissions management, and global health authority compliance standards before proceeding.
Kindly read the full job description carefully for your selected role before applying. Ensure your qualifications and profile align with centralized clinical trial data monitoring, risk indicators analysis, regulatory dossier compilation, lifecycle submissions management, and global health authority compliance standards before proceeding.
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