Are you looking to advance your career in clinical trial operations? A promising opportunity has opened for a Senior Associate – Clinical Trial Operations role in Bengaluru through Careernet. This position is ideal for professionals with 2–5 years of experience in clinical research, monitoring, and site management, especially those skilled in CTMS and TMF systems.
With increasing demand for skilled professionals in clinical operations jobs in India, this role offers hands-on exposure to trial lifecycle management, regulatory compliance, and site coordination.
🔬 Job Overview
- Role: Senior Associate – Clinical Trial Operations
- Company: Careernet
- Location: Bengaluru, India
- Experience: 2–5 Years
- Employment Type: Full-time
- Openings: 6
📌 Key Responsibilities
As a Senior Associate in Clinical Trial Operations, you will:
- Coordinate clinical trial documentation including IRB/IEC submissions
- Maintain and update CTMS (Clinical Trial Management System) and TMF (Trial Master File)
- Support site budget negotiations, contracts, and financial tracking
- Conduct quality control (QC) reviews to ensure audit readiness
- Monitor clinical trial progress and patient recruitment strategies
- Act as the primary point of contact for clinical trial sites
- Evaluate site performance, infrastructure, and compliance metrics
- Manage safety reporting as per regulatory guidelines
- Collaborate with cross-functional teams for issue resolution
- Support internal audits and regulatory inspections
- Build strong relationships with principal investigators and site staff
- Contribute to process improvement initiatives in clinical research
🎓 Qualifications & Skills Required
- Bachelor’s degree in:
- Life Sciences
- Pharmacy (B.Pharm / M.Pharm)
- Nursing
- Clinical Research or related field
Essential Skills:
- Strong knowledge of clinical trial operations and monitoring
- Hands-on experience with CTMS and TMF systems
- Understanding of ICH-GCP guidelines and regulatory compliance
- Experience with IRB/IEC submissions
- Familiarity with site budgeting and contract management
- Excellent documentation and audit readiness skills
- Ability to manage clinical site relationships and performance
- Strong communication and organizational abilities
💼 Salary & Benefits
- Estimated Salary Range: ₹6,00,000 – ₹10,00,000 per annum
- Exposure to global clinical trials and regulatory processes
- Opportunity to work with cross-functional clinical teams
- Career growth in clinical research and trial management
- Travel opportunities for site monitoring activities
🚀 Why This Role Matters
The demand for professionals in clinical trial operations jobs is rapidly increasing due to the growth of pharmaceutical and CRO industries in India. This role offers a solid pathway into advanced positions such as:
- Clinical Trial Manager
- Clinical Project Manager
- Regulatory Affairs Specialist
📥 How to Apply
