Labcorp, a global leader in healthcare and clinical research services, is inviting applications for the position of Senior Clinical Project Associate in Bangalore, India. This full-time opportunity is ideal for experienced clinical research professionals seeking to advance their careers in study maintenance, clinical operations support, and project documentation management within a reputed CRO environment.
This role plays a critical part in ensuring quality, compliance, and timely execution of clinical study activities, while collaborating closely with cross-functional teams and stakeholders.
๐ Job Overview
- Job Title: Senior Clinical Project Associate
- Company: Labcorp
- Location: Bangalore, India
- Employment Type: Full-time
- Job ID: 2542511
- Application Deadline: January 14, 2026
๐งช Key Responsibilities
As a Senior Clinical Project Associate, you will be responsible for:
- Following departmental SOPs and Work Instructions consistently
- Managing day-to-day clinical study maintenance tasks with high quality and productivity
- Handling project and technical documentation accurately
- Providing administrative and technical support to internal clinical teams
- Performing quality checks and responding to QC findings within defined timelines
- Tracking, maintaining, and reporting daily task metrics
- Acting as a single point of contact (POC) for process-related queries
- Ensuring 100% compliance with timesheets and training requirements
- Maintaining up-to-date training files in coordination with QADs
- Supporting process improvement initiatives
- Ensuring accurate data entry in daily task trackers
- Escalating issues proactively and supporting timely resolution
- Demonstrating leadership and acting as a role model within the study maintenance team
๐ Required Qualifications & Skills
- Bachelorโs or Masterโs degree in Life Sciences, Pharmacy, Clinical Research, or related discipline
- Relevant experience in clinical operations, study maintenance, or project coordination
- Strong understanding of clinical trial documentation and quality processes
- Experience working in a CRO or regulated clinical research environment
- Excellent communication, coordination, and organizational skills
- Ability to manage multiple tasks and meet strict timelines
๐ผ Salary & Benefits
- Estimated Salary: โน6,50,000 โ โน10,00,000 per annum (based on experience and industry standards)
- Competitive compensation package
- Exposure to global clinical research projects
- Structured training and career growth opportunities
- Inclusive, diverse, and equal opportunity workplace
- Strong focus on compliance, quality, and professional development
๐ How to Apply

