Regional Study Coordinator

Labcorp

. Act as regional liaison between the Global Study Manager and various LCLS departments involved in the study.

Posted 9/29/2026full-timeShanghai • ChinaJuniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing local study activities and liaising between global and local teams, ensuring compliance with project management strategies and operational specifications. Proficient in process improvement and maintaining high-quality standards in clinical trial operations.

Highest-signal resume keywords

Bachelor Degree In Life SciencesClinical Trial ManagementInterpersonal SkillsProcess Improvement InitiativesMicrosoft Office Proficiency

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial ManagementStudy Design ReviewLogistics ManagementPerformance Metrics ImplementationIssue Tracking and Resolution

Soft Skills

Strong Interpersonal SkillsInfluence And Negotiation SkillsCommunication SkillsOrganizational SkillsAttention To Detail

Tools & Technologies

Microsoft WordMicrosoft ExcelMS-AccessMicrosoft Outlook

Industry Keywords

Global Study ManagerStatement Of WorkLCLSMatrix EnvironmentContinuous Improvement

About the role

Key responsibilities & impact

Act as regional liaison between the Global Study Manager and various LCLS departments involved in the study.
Act as regional liaison between assigned client representatives and the corresponding local LCLS platform.
Collaborate with the Global Study Manager on study-related aspects throughout all study stages, from set-up to closure.
Review the study Statement of Work for local feasibility and make recommendations to the Study Design Lead.
Maintain detailed knowledge of Statement of Work specifications and their operational impact on the clinical trial.
Manage day-to-day local study activities, including logistics, monitoring and study supplies.
Monitor, track and resolve local study issues.
Implement monitoring, establish local performance metrics and take corrective actions when needed.
Liaise with the Global Study Manager on tasks assigned under the Global Monitoring Plan.
Work effectively in a matrix environment, completing assigned tasks and delegating tasks to functional groups.
Participate in functional meetings and provide input while keeping processes up to date.
Comply with the LCLS Global Project Management strategy.
Support continuous improvement, quality and productivity.
Interact regularly with internal stakeholders and occasionally with external clients.
Perform other duties as assigned.

Requirements

What you’ll need

Bachelor Degree in Life Sciences or Pharmaceuticals.
3 months or more experience using computer and office software applications (e.g. Microsoft Word, Excel, MS-Access and Outlook).
Proficiency in English. (Preferred Qualifications)
Strong interpersonal skills.
Influence and negotiation skills.
Demonstrated ability to plan and prioritize.
Demonstrated communication and organizational skills.
Demonstrated attention to detail.
Demonstrated participation in process improvement initiatives.
Proven ability to excel in a fast-paced environment.
Proven teamwork.
Proven experience and knowledge of processes and tools used in department.
Demonstrated ability to liaise with internal departments.
Demonstrated ability to facilitate meetings.

Benefits

Comp & perks

Equal Opportunity Employer commitment and non-discrimination
Accessibility assistance and workplace accommodation support for applicants with disabilities