MS Clinical Research is hiring Clinical Research Coordinators (CRC) in Delhi, India. This opportunity is ideal for professionals with 2โ4 years of experience in clinical research who want to work on clinical trials, study coordination, and regulatory compliance under ICH-GCP guidelines.
Clinical Research Coordinators play a critical role in managing clinical trial operations at research sites, ensuring proper documentation, supporting investigators, and coordinating with sponsors and ethics committees.
Candidates with Pharmacy, Life Sciences, Biotechnology, or related backgrounds who have experience working on clinical trial documentation, CRF management, and patient recruitment are encouraged to apply.
Job Overview
- Position: Clinical Research Coordinator (CRC)
- Company: MS Clinical Research
- Location: Delhi, India
- Experience Required: 2โ4 Years
- Employment Type: Full-time
- Industry: Clinical Research / Clinical Trials
- Work Mode: On-site
Key Responsibilities
The Clinical Research Coordinator will support clinical trial activities and ensure compliance with regulatory requirements.
Clinical Trial Operations
- Conduct clinical trials in accordance with ICH-GCP guidelines and study protocols
- Support study start-up activities including site initiation and documentation
- Assist investigators in subject recruitment and retention
Documentation & Compliance
- Maintain accurate source documents, Case Report Forms (CRFs), and study logs
- Compile and update the Site Master File (SMF) and regulatory documentation
- Ensure compliance with clinical trial protocols and regulatory standards
Investigational Product Management
- Manage Investigational Product (IP) accountability and shipping
- Maintain drug accountability logs and storage compliance
Regulatory & Sponsor Coordination
- Coordinate Ethics Committee submissions and approvals
- Provide updates to clinical trial sponsors on study progress
- Prepare for monitoring visits, audits, and inspections
Eligibility Criteria
Candidates interested in the Clinical Research Coordinator job in Delhi should meet the following requirements:
Education
- Bachelorโs or Masterโs degree in:
- Pharmacy (B.Pharm / M.Pharm)
- Life Sciences
- Biotechnology
- Related healthcare disciplines
Experience
- Minimum 2 years of experience as a Clinical Research Coordinator
Skills Required
- Knowledge of ICH-GCP guidelines
- Clinical trial documentation and regulatory understanding
- Strong communication and organizational skills
- Ability to manage clinical study documentation and subject coordination
Benefits of Joining MS Clinical Research
Working as a Clinical Research Coordinator at MS Clinical Research provides an opportunity to build a career in the growing clinical trials industry.
Key advantages include:
- Hands-on experience in clinical trial operations
- Exposure to global clinical research protocols and compliance
- Opportunity to work with experienced investigators and research professionals
- Career growth in clinical research, site management, and regulatory operations
How to Apply
