Study Design Lead

Labcorp

. Interpret and translate sponsor protocol requirements into protocol-specific databases and generate Statements of Work for Central Lab Services projects .

Posted 9/21/2026full-timeRemote • United KingdomSeniorWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in clinical research project management, including protocol interpretation, database design, and client relationship management. Proficient in coordinating study design processes and ensuring compliance with project management strategies.

Highest-signal resume keywords

Clinical Research ExperienceDatabase DesignClient Relationship ManagementProject ManagementProblem-Solving Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Protocol InterpretationDatabase DesignStudy DesignFeasibility AssessmentQuality Review

Soft Skills

Relationship BuildingOrganizational SkillsCommunication SkillsPlanning Skills

Tools & Technologies

WindowsExcelWord

Industry Keywords

Clinical ResearchCentral Lab ServicesPreclinical ResearchStudy DesignProject Management Strategy

About the role

Key responsibilities & impact

Interpret and translate sponsor protocol requirements into protocol-specific databases and generate Statements of Work for Central Lab Services projects
Provide comprehensive database designs using technical, therapeutic-area, client, and company process knowledge
Interact regularly with external clients
Liaise with internal departments to assess feasibility and meet client study-design needs
Advise on study-design choices and work with the Global Study Manager to identify risks and budget impacts
Build strong internal and external relationships to ensure high-quality study design
Coordinate internal study-design processes and communications, including feasibility requests, material transfer agreements, and supply forecasting
Integrate follow-up into databases and global monitoring plans and perform quality self-review
Document and act on customer study-design requirements
Manage dynamic timelines, competing priorities, and a portfolio of global and local studies of varying complexity
Participate in functional meetings and contribute to keeping processes current
Comply with the Central Lab Global Project Management strategy
Support continuous improvement, quality, and productivity

Requirements

What you’ll need

Bachelor’s degree in a life science
6 or more years of experience working in the clinical research industry or within a lab environment
Experience working directly with internal or external customers
Strong relationship building and management skills
Familiarity with clinical or preclinical research protocols
Strong planning, organizational, and problem-solving skills
Excellent verbal and written communication skills
Excellent skills using computer applications, including Windows, Excel, and Word
Preferred: Master degree in a life science
Preferred: 6 or more years experience in Central Lab Project management

Benefits

Comp & perks

Equal Opportunity Employer commitment
Consideration of qualified applicants without regard to protected characteristics
Accessibility assistance and reasonable accommodation for applicants with disabilities