Labcorp
healthcare
SrClinicalProjectAssociate
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“Sr Clinical Project Associate at Labcorp. Skills: process management, cross-functional coordination, vendor/stakeholder management. Follow departmental SOPs and Work Instructions. Complete required trainings”
What You'll Achieve.
quality and productivity; timely escalation and issue resolution; 100% compliance weekly; accuracy of data entered
Industry & Context.
issue resolution
What They're Looking For.
Must Have
Bachelor's Degree in Life Science
Nice to Have
4 years of experience working in the clinical research industry
What You'll Do.
Follow departmental SOPs and Work Instructions
Complete required trainings
Manage day-to-day tasks
Manage project and technical documentation
Provide administrative and technical support
Perform checks to ensure quality
Ensure timely escalation and issue resolution
Track and report metrics
Participate in process improvement opportunities
Assist with implementation of revised processes
Collaborate with workload dealer
Ensure assigned tasks completed within timelines
Respond to quality issues within 1 day
Ensure timesheet and training compliance
Ensure training files are up to date
Ensure accuracy of data entered
Notify managers when defaults identified
Be single POC for process questions
Work on additional tasks as requested
How You'll Work.
Team & Collaboration
Collaborate with the workload dealer; Work with the manager; Work with QADs; Be the single POC for the team; Be a role model for the team
Communication Scope
communicate effectively
Process & Methodology
Manage project and technical documentation, Ensure timely escalation and issue resolution, Track and report metrics
Full Job Description
Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives. LabCorp is seeking a Sr Clinical Project Associate to join our team at Brigade Twin Tower in Bangalore, Karnataka. **Work Schedule** Rotating shift - 5-day working mode **Minimum Qualifications** Bachelor's Degree in Life Science **Preferred Qualifications** 4 years of experience working in the clinical research industry **Job Responsibilities** · Follow applicable departmental Standard Operating Procedures and Work Instructions. · Complete required trainings according to required timelines. · Manage day-to-day tasks ensuring quality and productivity. · Manage project and technical documentation in an appropriate manner. · Provide administrative and technical support to internal departments as needed. · Perform checks to ensure quality of work completed. · Ensure timely escalation and issue resolution. · Track and report metrics as determined by management according to required timelines. · Participate in process improvement opportunities and assist with the implementation of revised processes and procedures. · Collaborate with the workload dealer and ensure all assigned tasks are completed within specified timelines. · Ensure quality issues identified by the QC reviewer are responded to within 1 day of being notified. · Work with the manager to ensure timesheet and training compliance for all staff within the teams are at 100% every week. · Work with QADs and ensure the training files are up to date. · Ensure accuracy of data entered on the Daily task tracker and notify managers when defaults are identified. · Be the single POC for the team in terms of the process questions along with the SMEs. · Work on additional tasks and requirements as requested by the manager from time to time. · Be a role model for the team in terms of d
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