Are you ready to step into the world of clinical trials and medical innovation?
Med Express Clinical Research Solutions Private Limited has announced fresh openings for Clinical Research Coordinators (CRC) in Vadodara (Gujarat) and Lucknow (Uttar Pradesh).
This is an excellent opportunity for Pharm D, B.Pharm, and M.Pharm graduates with 6 months to 1 year of experience who want to build a long-term career in clinical research.
🧬 What Does a Clinical Research Coordinator (CRC) Do?
A Clinical Research Coordinator plays a critical role in ensuring that clinical trials run smoothly, ethically, and in compliance with regulations.
Think of the CRC as the bridge between doctors, patients, sponsors, and regulatory bodies. While Principal Investigators focus on medical decisions, CRCs manage documentation, patient coordination, and protocol compliance.
This role is ideal if you enjoy:
- Patient interaction
- Medical science
- Structured documentation
- Regulatory and ethical compliance
📊 Job Details at a Glance
- Position: Clinical Research Coordinator (CRC)
- Company: Med Express Clinical Research Solutions Pvt. Ltd.
- Qualification: Pharm D / B.Pharm / M.Pharm
- Experience Required: 6 months – 1 year (Mandatory)
- Job Locations:
- Vadodara, Gujarat
- Lucknow, Uttar Pradesh
- Application Email: hr@mecrsindia.com
📝 Roles & Responsibilities of a CRC
1️⃣ Participant Recruitment & Management 👥
- Identify eligible trial participants
- Explain study objectives and procedures
- Guide participants through Informed Consent (ICF)
- Ensure patient comfort and compliance throughout the study
2️⃣ Protocol Compliance & Documentation 📂
- Maintain accurate Case Report Forms (CRFs)
- Ensure strict adherence to study protocols
- Follow Good Clinical Practice (GCP) guidelines
3️⃣ Site Coordination & Sample Handling 🧪
- Schedule patient visits
- Coordinate lab sample collection and shipment
- Maintain trial supplies and logs
4️⃣ Regulatory & Ethics Support ⚖️
- Maintain Investigator Site File (ISF)
- Coordinate with Ethics Committees
- Support audits and monitoring visits
🚀 Why Join Med Express Clinical Research Solutions?
- Early Career Breakthrough: Ideal for candidates with initial clinical research exposure
- CRO Experience: Learn how global trials are managed end-to-end
- Regional Growth: Vadodara and Lucknow are fast-emerging clinical research hubs
- Strong Learning Curve: Excellent foundation for CRA, PM, or Regulatory roles
🎯 How to Apply (Pro Tips That Work)
📧 Send your CV to: hr@mecrsindia.com
Use this subject line:
Application for CRC – [Vadodara/Lucknow] – [X Years Experience]
✅ Application tips:
- Mention clinical trials or internships clearly
- Highlight GCP certification (very important!)
- State notice period / immediate availability
- Local candidates get preference
📈 Career Growth After CRC Role
The CRC position is a launchpad to roles like:
- Clinical Research Associate (CRA)
- Project Manager – Clinical Trials
- Regulatory Affairs Executive (CDSCO, DCGI exposure)
- Clinical Data Management
With experience, these roles can lead to high-paying global opportunities 🌍
