Clinical Research Coordinator

Roles & Responsibilities
• Manage day-to-day clinical trial operations at the site
• Collect, record, and update clinical trial data daily
• Share weekly study progress and data collection reports with stakeholders
• Handle data queries and ensure timely resolution
• Support monitoring visits, audits, and regulatory inspections
• Coordinate patient follow-ups to ensure protocol compliance
• Maintain essential documents and source data integrity
• Liaise with investigators, site staff, sponsors, and CRO teams

Qualification
• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related discipline

Experience
• Prior experience as a Clinical Research Coordinator is preferred
• Oncology clinical research experience will be an added advantage

Skills
• Strong understanding of clinical trial processes, ICH-GCP, and regulatory guidelines
• Excellent communication, documentation, and organizational skills
• Ability to manage multiple studies independently

About the Company
Micro Data Labs is a clinical research organization committed to advancing scientific research and improving patient outcomes. The company provides comprehensive support for clinical trials, focusing on quality, compliance, and operational excellence. Micro Data Labs fosters a collaborative environment where professionals can grow in clinical research and contribute meaningfully to healthcare advancements.

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Email ID: careers@microdatalabs.com