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 • BulgariaSeniorWebsite

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. Proficient in managing timelines and priorities while ensuring compliance with Central Lab strategies and continuous improvement initiatives.

Highest-signal resume keywords

Clinical Research ExperienceCentral Lab Project ManagementDatabase DesignClient Relationship ManagementProblem-Solving Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Protocol InterpretationDatabase DesignStudy DesignQuality Self-ReviewFeasibility AssessmentSupply ForecastingProject ManagementClinical Research Protocols

Soft Skills

Relationship BuildingOrganizational SkillsCommunication Skills

Tools & Technologies

WindowsExcelWord

Industry Keywords

Life Science DegreeClinical Research IndustryPreclinical Research

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
Provide comprehensive database designs using technical, therapeutic area, client, and company-specific process knowledge
Interact regularly with external clients
Liaise with internal departments to assess feasibility and meet client needs related to study design
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 into databases and global monitoring plans; perform quality self-review
Document and act on customer study-design requirements
Manage dynamic timelines, conflicting priorities, and a portfolio of global and local studies of varying complexity
Participate in functional meetings and contribute to keeping processes up to date
Comply with 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
Preferred: Master degree in a life science
Preferred: 6 or more years experience in Central Lab Project management
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

Benefits

Comp & perks

Equal Opportunity Employer commitment
Reasonable accommodations for individuals with disabilities during online application
Global career growth opportunity
Opportunity to do meaningful work and make a real impact on people’s health