MS Clinical Research Pvt Ltd is inviting applications for the position of Senior Clinical Research Associate (Sr. CRA) in Delhi. This Clinical Research Associate job in Delhi is ideal for professionals with at least 3 years of experience in clinical trial monitoring, site management, and regulatory compliance under ICH-GCP guidelines.
If you are looking for a Clinical Research Associate job in India with strong exposure to monitoring visits, regulatory documentation, and safety reporting, this opportunity offers career growth in a reputed clinical research organization.
About MS Clinical Research Pvt Ltd
MS Clinical Research (MSCR) is a leading Clinical Research Organization (CRO) committed to conducting high-quality clinical trials in compliance with global regulatory standards. The organization focuses on scientific innovation, regulatory excellence, and maintaining the highest standards of data integrity in clinical research.
Job Details
- Position: Senior Clinical Research Associate (Sr. CRA)
- Location: Delhi, India
- Experience Required: Minimum 3 Years
- Industry: Clinical Research / CRO
- Employment Type: Full-Time
- Travel Requirement: Extensive site travel
Key Responsibilities
1. Site Management & Monitoring
- Conduct Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Close-Out Visits (COV)
- Ensure compliance with ICH-GCP, study protocols, and regulatory guidelines
- Build strong relationships with investigators and site coordinators
- Identify and resolve site-related issues proactively
2. Clinical Trial Oversight
- Perform Source Data Verification (SDV)
- Ensure protocol adherence and data accuracy
- Support Risk-Based Monitoring (RBM) strategies
- Follow up on monitoring findings and query resolution
3. Regulatory & Compliance
- Assist in regulatory submissions and ethics committee communications
- Maintain documentation as per SOPs and international guidelines
- Stay updated with evolving regulatory requirements
4. Safety & Pharmacovigilance Coordination
- Monitor and report Adverse Events (AEs) and Serious Adverse Events (SAEs)
- Ensure timely safety reporting as per regulatory timelines
5. Quality & Mentorship
- Support audit readiness and corrective actions
- Mentor junior CRAs and site staff
- Serve as a subject matter expert for operational queries
Qualifications Required
- Bachelor’s or Master’s degree in Life Sciences or related field
- Minimum 3 years experience as a Clinical Research Associate
- Strong knowledge of ICH-GCP guidelines
- Understanding of clinical trial monitoring and site management
- Experience in regulatory documentation and safety reporting
Required Skills
- Excellent communication and interpersonal skills
- Strong analytical and problem-solving abilities
- Good documentation and reporting expertise
- Ability to work independently and in cross-functional teams
- Willingness to travel to investigative sites
Salary & Benefits
- Estimated Salary Range: ₹5.5 LPA – ₹8.5 LPA (Based on experience)
- Competitive compensation package
- Professional growth opportunities
- Leadership development exposure
- Collaborative and innovation-driven work environment
Why This Clinical Research Associate Job is Important
The role of a Senior Clinical Research Associate is critical in ensuring regulatory compliance, patient safety, and data integrity in clinical trials. With growing demand for skilled CRAs in India, this Delhi-based opportunity offers strong career progression in the clinical research domain.
How to Apply
