Study Design Lead – Clinical Research, Central Labs Services

Labcorp

. Interpret sponsor protocol requirements and translate them into precise, study-specific database designs for CLS projects .

Posted 9/17/2026full-timeRemote • United StatesSenior💰 $70,000 - $90,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical and preclinical research protocols, with a strong focus on database design and client engagement. Capable of managing complex study portfolios while ensuring quality and compliance with sponsor requirements.

Highest-signal resume keywords

Clinical Research ExperienceDatabase DesignClient EngagementQuality AssuranceAnalytical Problem-Solving

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Database DesignClinical Research ProtocolsFeasibility AssessmentStudy Design DocumentationSupply Forecasting

Soft Skills

Verbal CommunicationWritten CommunicationRelationship ManagementOrganizational SkillsProblem-Solving

Industry Keywords

Clinical ResearchPreclinical ResearchStudy DesignClient Stakeholder EngagementGlobal Study Management

About the role

Key responsibilities & impact

Interpret sponsor protocol requirements and translate them into precise, study-specific database designs for CLS projects
Apply technical, therapeutic area, client, and CLS process knowledge to deliver complete and accurate database designs
Engage with external clients throughout study design and development
Partner with internal departments to evaluate feasibility of client study design requests
Advise on study design decisions with the Global Study Manager, including risks and budget implications
Coordinate feasibility assessments, material transfer agreements, supply forecasting, and related communications
Incorporate follow-up actions into the database and global monitoring plan
Conduct thorough quality self-review
Document and address all client study design requirements
Manage a diverse portfolio of global and local studies with varying complexity

Requirements

What you’ll need

High School Diploma
7 or more years of professional experience working in clinical or preclinical research
1 or more years of experience working directly with clients and stakeholders
Familiarity with clinical or preclinical research protocols
Strong scientific acumen with an investigative, analytical mindset
Strong planning, organizational, and problem-solving capabilities
Excellent verbal and written communication skills
Proven relationship-building and relationship-management skills
Ability to manage shifting timelines, evolving priorities, and competing demands
Bachelor’s degree in life sciences (preferred)
2 or more years of experience working directly with clients and stakeholders (preferred)

Benefits

Comp & perks

Medical insurance
Dental insurance
Vision insurance
Life insurance
Short-term disability (STD)
Long-term disability (LTD)
401(k)
Paid Time Off (PTO) or Flexible Time Off (FTO)
Tuition Reimbursement
Employee Stock Purchase Plan