Full Time

Clinical Research Coordinator

Micro Data Labs
Delhi NCR
₹2.5 - ₹4 LPA
Posted 09/01/2026

About the Role

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.


AI Career Power Suite

Resume Analyst

Unlock refined AI insights.

Interested?

Frequently Asked Questions

Everything you need to know about the process

Click the 'Apply Now' button on the job details page. You can apply as a guest or create an account to track your applications.
Yes! Jobslly is 100% free for healthcare professionals looking for jobs.
You can subscribe to our weekly newsletter or create an account to receive personalized job recommendations.
Most employers require a resume, but some entry-level positions may allow you to apply with just a profile summary.
Log in to your dashboard and navigate to the 'Profile' section to update your details and resume.
Yes, we verify all employers and job postings to ensure they are legitimate opportunities.