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Clinical Project Associate | Labcorp

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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.


๐Ÿ“Œ 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

๐Ÿงช Key Responsibilities

As a Senior Clinical Project Associate, you will be responsible for:

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  • 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

๐ŸŽ“ Required Qualifications & Skills

  • Bachelorโ€™s or Masterโ€™s 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

๐Ÿ’ผ Salary & Benefits

  • Estimated Salary: โ‚น6,50,000 โ€“ โ‚น10,00,000 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

๐Ÿ“ How to Apply

Application Link

Clinical Project Associate | Labcorp
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