Clinical Research Coordinator - Delhi

MS Clinical Research; Delhi; On-site; INR 400,000 - 600,000; Full time

Benefits offered by this job

Hands-on experience in clinical trials

Learn from experienced professionals

Opportunities for career growth

Job summary

MS Clinical Research in Delhi is looking for passionate Clinical Research Coordinators (CRCs) to join their team. This full-time role is ideal for candidates with 2-4 years of experience in clinical research or those with a background in life sciences/pharmacy, paired with clinical research certification.

The position involves managing clinical study activities and ensuring compliance with protocols while maintaining high documentation standards. Apply now for an exciting career in clinical trials!

Qualifications

• 2–4 years of experience in clinical research or certification in clinical research.
• Strong interest in clinical trials and regulatory compliance.
• Ability to manage documentation and data integrity.

Responsibilities

• Conduct clinical trials in compliance with ICH GCP and protocol guidelines.
• Support study start-up activities and assist with site initiation.
• Coordinate submissions and communicate with the Ethics Committee.

Skills

Organizational skills

Communication skills

Documentation skills

Education

Graduates/postgraduates in Life Sciences, Pharmacy, or Biotechnology

Job description

We are looking for passionate and detail-oriented Clinical Research Coordinators (CRCs) to join our growing team. This is an exciting opportunity for professionals with 2–4 years of experience in clinical research, or for those with a background in life sciences/pharmacy and a certification in clinical research, who aspire to build a strong career in clinical trials and research operations.

The CRC will play a key role in managing clinical study activities, ensuring protocol compliance, and maintaining high standards of documentation and data integrity.

Role: Clinical Research Coordinator

Employment Type: Full-time

Experience: 2-4 Years

Key Responsibilities

• Conduct clinical trials in compliance with ICH GCP and protocol guidelines.
• Support study start-up activities and assist with site initiation.
• Participate in recruitment and retention of study subjects.
• Complete and maintain source documents, CRFs, and logs accurately.
• Compile and update the Site Master File.
• Manage Investigational Products (IP), including accountability and shipping.
• Coordinate submissions and communication with the Ethics Committee.
• Update sponsors on study progress and prepare for monitoring visits.
• Perform other responsibilities assigned by management.

Who Can Apply

• Freshers with a completed Clinical Research course.
• Graduates/postgraduates in Life Sciences, Pharmacy, Biotechnology, or related fields.
• Strong interest in clinical trials and regulatory compliance.
• Excellent organizational, communication, and documentation skills.

Why Join Us?

• Gain hands-on experience in clinical trials.
• Learn directly from experienced professionals.
• Be part of innovative projects that shape the future of healthcare.
• A great opportunity to grow your career in clinical research.