Roles & Responsibilities
• Coordinate and manage day-to-day clinical trial activities
• Assist investigators during subject screening, enrollment, and follow-up visits
• Maintain essential trial documentation in compliance with ICH-GCP guidelines
• Ensure protocol adherence and accurate, timely data collection
• Liaise with sponsors, CROs, ethics committees, and study stakeholders
• Support monitoring visits, audits, and regulatory inspections
• Ensure subject safety, data integrity, and ethical conduct of studies
Qualification
• M.Sc in Life Sciences
• B.Pharm / M.Pharm
• Nursing or other related healthcare disciplines
Experience
• Prior experience in clinical research or clinical trials preferred
• Freshers with strong interest in clinical research are encouraged to apply
Skills
• Working knowledge of ICH-GCP and clinical trial regulations
• Strong documentation and coordination skills
• Good communication and organizational abilities
• Attention to detail and ability to manage multiple tasks
About the Organisation
Siaram Research is a growing clinical research organization committed to ethical research practices, regulatory compliance, and scientific excellence. The organization provides a supportive and growth-oriented environment for professionals aiming to build a long-term career in clinical research and healthcare research coordination.
Send your CV to: Shekhar@siaramresearch.com
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