Clinical Research Coordinator Job Opportunities at Micro Data Labs
- Clinical Research Coordinator Jobs in Chennai – Immediate Hiring for CRC Roles (Apply Before 30 April)
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What does a Clinical Research Coordinator do?
- What is the career growth after CRC?
- Is CRC a good career option?
- Summary
Clinical Research Coordinator Jobs in Chennai – Immediate Hiring for CRC Roles (Apply Before 30 April)
A clinical research site in Chennai is urgently hiring Clinical Research Coordinator (CRC) professionals for immediate joining. This is a full-time opportunity for candidates interested in clinical trials, patient coordination, and clinical data management.
The opening is ideal for candidates with a background in life sciences, pharmacy, or nursing who want to build a career in clinical research and site management. Applications close on 30 April 2026.
Company Overview
Micro Data Labs is involved in clinical research operations, supporting clinical trial execution, data collection, and regulatory compliance. The organization works closely with sponsors, investigators, and healthcare teams to ensure accurate clinical data and smooth trial conduct.
With a focus on quality, compliance, and patient safety, the company contributes to advancing clinical research and supporting drug development processes.
Job Role & Responsibilities
As a Clinical Research Coordinator (CRC), you will manage site-level clinical trial activities and ensure compliance with protocols and regulatory guidelines.
Core Responsibilities
- Manage daily clinical trial operations at the study site
- Collect, record, and maintain accurate clinical trial data
- Prepare weekly progress reports and data updates for stakeholders
- Handle data queries and ensure timely resolution of discrepancies
- Support audits, monitoring visits, and regulatory inspections
- Conduct patient follow-ups to ensure protocol adherence
- Maintain documentation and ensure data integrity throughout the study
- Coordinate with investigators, sponsors, and site staff
Eligibility / Qualifications
- Educational Qualification: B.Pharm, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Nursing or related field
- Experience: Prior experience as Clinical Research Coordinator preferred
- Good understanding of clinical trials, GCP guidelines, and regulatory requirements
- Strong communication, documentation, and organizational skills
- Ability to handle multiple tasks and work independently
Location & Salary
- Job Location: Chennai, Tamil Nadu, India
- Work Mode: On-site
- Salary Range: ₹2.8 LPA – ₹5.5 LPA (approximate based on CRC roles in India)
This range reflects entry to mid-level clinical research coordinator salaries depending on experience and site type.
Application Process
Interested candidates should apply via email:
Email: careers@microdatalabs.com
Subject Line: Chennai: CRC Application
Apply before 30 April 2026. Immediate joiners will be preferred.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
Freshers may apply if they have relevant academic exposure, but prior CRC experience is preferred.
What does a Clinical Research Coordinator do?
A CRC manages clinical trial activities at the site, including patient coordination, data collection, and regulatory compliance.
What is the career growth after CRC?
You can move into CRA, Clinical Project Management, or Regulatory Affairs roles.
Is CRC a good career option?
Yes, CRC roles are a strong entry point into the clinical research and CRO industry.
Summary
| Category | Details |
|---|---|
| Company | Micro Data Labs |
| Vacancies | Clinical Research Coordinator (CRC) |
| Required Education | B.Pharm, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Nursing |
| Experience | Preferred CRC experience (freshers may apply) |
You must sign in to apply for this position.