MS Clinical Research Pvt Ltd (MSCR), a reputed Clinical Research Organization (CRO) in India, has announced multiple clinical research job openings for 2026. The company is inviting applications for the following full-time positions:
- Research Assistant – Instrumentation (Delhi)
- Clinical Research Coordinator – CRC (Delhi)
- Clinical Research Associate – CRA (Bangalore)
These opportunities are ideal for freshers and experienced professionals looking to build or advance a career in clinical trials, ICH-GCP compliance, and research operations.
Primary Keywords:
MS Clinical Research jobs, Clinical Research jobs in Delhi, Clinical Research Associate jobs, CRC jobs India
1. Research Assistant – Instrumentation (Delhi)
Job Summary
The Research Assistant – Instrumentation will support clinical trial execution through instrument handling, calibration, documentation, and coordination, ensuring compliance with ICH-GCP, study protocols, and SOPs.
Key Responsibilities
- Conduct clinical trial activities as per ICH-GCP guidelines
- Operate, maintain, and calibrate clinical instruments
- Maintain accurate calibration and instrument records
- Coordinate with floor teams for study execution
- Schedule subjects and ensure protocol adherence
- Report deviations and operational issues to management
Eligibility & Skills
- Bachelor’s degree or diploma in Life Sciences / Pharmacy
- 0–2 years experience (freshers can apply)
- Knowledge of clinical research instrumentation
- Strong documentation and coordination skills
2. Clinical Research Coordinator (CRC) – Delhi
Job Overview
MSCR is hiring Clinical Research Coordinators to manage site-level clinical trial activities, ensuring regulatory compliance, data integrity, and smooth study operations.
Key Responsibilities
- Conduct trials in compliance with ICH-GCP & protocols
- Assist in site initiation and ethics submissions
- Subject recruitment and retention
- Maintain source documents, CRFs, and Site Master File
- Manage Investigational Product (IP) accountability
- Coordinate sponsor communication and monitoring visits
Who Can Apply
- Graduates/Postgraduates in Life Sciences, Pharmacy, Biotechnology
- Freshers with Clinical Research certification
- 1–4 years of clinical research experience preferred
- Strong interest in regulatory and clinical operations
3. Clinical Research Associate (CRA) – Bangalore
Job Summary
The Clinical Research Associate will oversee site monitoring, compliance, safety reporting, and regulatory coordination, ensuring successful clinical trial delivery.
Key Responsibilities
- Conduct site initiation, monitoring, and close-out visits
- Perform source data verification (SDV)
- Ensure protocol and regulatory compliance
- Monitor adverse events and safety reporting
- Train site staff on protocols and GCP
- Coordinate with data management and regulatory teams
Eligibility Criteria
- Bachelor’s degree in Life Sciences or related field
- Minimum 3 years CRA experience
- Strong knowledge of GCP and clinical regulations
- Willingness to travel across sites
Why Join MS Clinical Research Pvt Ltd?
- Exposure to high-quality clinical trials
- Career growth in a regulated CRO environment
- Work with experienced clinical research professionals
- Competitive salary and structured learning opportunities
How to Apply
Application Link for Research Assistant – Instrumentation (Delhi)
Application Link for Clinical Research Coordinator (CRC) – Delhi
Application Link for Clinical Research Associate (CRA) – Bangalore
