Looking for high-growth careers in clinical research, pharmacovigilance, and medical affairs? Syngene International is actively hiring for Medical Monitor and Clinical Study Manager roles in India.
This is a strong opportunity for professionals aiming to work on global clinical trials, patient safety, and regulatory compliance while collaborating with cross-functional teams in a CRO environment.
๐ง Role 1: Manager โ Medical Monitor (Bengaluru)
๐ฌ Key Responsibilities
- Provide medical oversight for clinical trials including AE/SAE review
- Interpret clinical and safety data ensuring scientific accuracy
- Draft Integrated Summary of Safety & Efficacy (ISS/ISE)
- Support protocol design, Investigatorโs Brochure, and CSR
- Conduct MedDRA & WHO Drug coding reviews
- Develop Medical Monitoring Plans (MMP) and REMS
- Communicate safety updates to stakeholders within timelines
- Travel to sites for monitoring and clinical evaluation
๐ฏ Qualifications
- MBBS + MD (Pharmacology preferred)
- Strong knowledge of ICH-GCP, pharmacovigilance, and clinical trials
- Experience in AE/SAE assessment, safety narratives, and regulatory compliance
๐ก Why This Role Matters
This role sits at the intersection of clinical research + pharmacovigilance, ensuring:
- Patient safety
- Ethical compliance
- Data integrity
๐ Source:
๐ Role 2: Clinical Study Manager (India)
๐งฉ Key Responsibilities
- Lead end-to-end clinical trial management
- Coordinate with sponsors, CRO teams, and vendors
- Develop Project Management Plans & study timelines
- Monitor CRA performance and site activities
- Ensure protocol compliance, data quality, and audit readiness
- Handle risk management, issue resolution, and escalation
- Participate in feasibility, budgeting, and proposal development
๐ฏ Qualifications
- Degree in Life Sciences / Pharmacy
- Experience in clinical operations / trial management
- Strong stakeholder management & leadership skills
๐ก Core Impact
This role drives:
- Operational excellence in clinical trials
- Timely study delivery
- Compliance with regulatory frameworks
๐ Source:
๐ฐ Salary Insights (India โ Estimated)
- Medical Monitor: โน18โ35 LPA
- Clinical Study Manager: โน12โ25 LPA
(Based on industry benchmarks for CRO roles in India)
๐ Benefits of Working at Syngene
- Exposure to global clinical trials
- Strong learning in ICH-GCP, PV, regulatory affairs
- Cross-functional collaboration with global stakeholders
- Career growth in CRO & pharmaceutical ecosystem
- Safety-first organizational culture
๐ How to Apply
Application Link For Manager โ Medical Monitor (Bengaluru)
Application Link For Clinical Study Manager (India)
