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Role & Responsibilities
• Ensure smooth day-to-day operations of clinical trials at the site
• Collect, review, and update clinical trial data daily
• Share weekly updates on data collection and trial progress
• Manage query response and ensure timely resolution
• Coordinate patient follow-ups and visit schedules
• Maintain compliance with ICH-GCP, SOPs, and regulatory requirements
• Support investigators and sponsors during trial execution
Qualifications & Experience
• B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy)
• 0-3 years of experience in clinical research or clinical trials
• Sound knowledge of ICH-GCP guidelines
• Good documentation and data management skills
• Strong communication and coordination abilities
About the Company
• Micro Data Labs is a leading Clinical Research Organization (CRO), providing clinical trial management and operations in compliance with ICH-GCP guidelines.