Research Assistant- Instrumentation

Roles & Responsibilities
• Conduct trials in accordance with ICH-GCP and protocol-specified guidelines
• Operate, handle, and maintain instruments as per SOPs and instrument manuals
• Perform and support SPF and Hair In-vitro studies as per study requirements
• Document instrument readings and study data accurately and in a timely manner
• Calibrate instruments within defined timelines and maintain calibration and maintenance records
• Coordinate day-to-day study activities on the floor and support smooth trial execution
• Assist in scheduling subjects for study visits and coordinating visit flow
• Submit study-related data for analysis within agreed timelines
• Identify, report, and escalate concerns/anomalies to the line manager, and follow up until resolution

Qualification
• Degree in Life Sciences, Pharmacy, or related field

Experience
• 2 to 6 years of relevant experience in clinical trials/study conduct as per ICH-GCP
• Hands-on experience with instrument operation, handling, and maintenance preferred

Skills
• ICH-GCP and protocol compliance awareness
• Instrument handling, SOP adherence, and calibration documentation
• Strong data recording and documentation discipline
• Good coordination and organizational skills for study floor activities
• Effective communication, reporting, and issue escalation skills

About The Company
MS Clinical Research supports clinical research and study execution aligned with regulated quality standards, focusing on compliant trial conduct, accurate documentation, and operational coordination across study activities.