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Sr Clinical Project Coordinator

Labcorp
2+ years
Not Disclosed
Bangalore, India
1 June 2, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Sr Clinical Project Coordinator

Company: Labcorp
Location: Bangalore, Karnataka, India
Department: Clinical Operations
Job Type: Full-Time (Office-Based)
Work Schedule: Rotating Shift | 5-Day Working Model

Role Summary

The Sr Clinical Project Coordinator is responsible for supporting clinical project operations through effective documentation management, process compliance, quality oversight, training coordination, and administrative support. The role ensures timely project execution while maintaining adherence to SOPs, work instructions, and quality standards.


Key Responsibilities

Project Coordination & Operations

  • Manage day-to-day project activities while ensuring quality and productivity.

  • Maintain project and technical documentation in an organized and compliant manner.

  • Provide administrative and operational support to internal departments.

  • Perform quality checks on completed work to ensure accuracy and compliance.

  • Ensure timely escalation and resolution of project-related issues.

  • Support additional project activities and assignments as directed by management.

Training & Knowledge Management

  • Complete all required training programs within defined timelines.

  • Plan and deliver training sessions for team members.

  • Prepare training agendas, materials, and supporting documentation.

  • Support onboarding and continuous learning initiatives.

SOP & Process Management

  • Follow departmental Standard Operating Procedures (SOPs) and Work Instructions (WIs).

  • Create, review, and update SOPs and WIs as required.

  • Assess process effectiveness and recommend improvements.

  • Ensure timely submission of version-controlled documents to the Global QA SOP team.

Quality & Compliance

  • Ensure compliance with company policies, SOPs, and quality standards.

  • Support process improvement initiatives and implementation of revised procedures.

  • Maintain accurate records and documentation for audit readiness.


Required Qualifications

Education

  • Bachelor's Degree in Life Sciences or a related field.

Experience

  • Minimum 2 years of experience in the Clinical Research industry (preferred).