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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.
