Study Design Lead

Labcorp

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

Posted 9/21/2026full-timeRemote • BelgiumSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research project management, including protocol interpretation, database design, and client interaction. Strong capabilities in planning, organization, and communication are essential for managing complex study designs and timelines.

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 DesignClinical Research ProtocolsProject ManagementQuality Self-Review

Soft Skills

Relationship BuildingOrganizational SkillsVerbal CommunicationWritten CommunicationPlanning Skills

Tools & Technologies

WindowsExcelWord

Industry Keywords

Clinical ResearchCentral Lab ServicesStudy DesignFeasibility AssessmentMaterial Transfer Agreements

About the role

Key responsibilities & impact

Interpret and translate sponsor protocol requirements into protocol-specific databases to generate Statements of Work for Central Lab Services projects
Leverage technical, therapeutic-area, client, and company process knowledge to create comprehensive database designs
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
Coordinate internal study-design processes and communications, including feasibility requests, material transfer agreements, and supply forecasting
Integrate follow-up activities into databases and global monitoring plans
Document and act on customer study-design requirements
Manage dynamic timelines, conflicting priorities, and a portfolio of global and local studies with varying complexities
Participate in functional meetings and contribute to keeping processes current
Perform quality self-review and support continuous improvement, quality, and productivity
Comply with the Central Lab Global Project Management strategy

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 and consideration without regard to legally protected characteristics
Disability accommodations for applicants using online tools
Global career growth and meaningful work opportunities