FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research project management, including study design, protocol-specific database creation, and client relationship management. Proficient in coordinating complex study processes while ensuring compliance with project management strategies.
Highest-signal resume keywords
Clinical Research Project ManagementProtocol-Specific Database DesignClient Relationship ManagementStudy Design TechniquesQuality Self-Reviews
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Database DesignStudy Design TechniquesProtocol Requirements InterpretationProject ManagementFeasibility AssessmentBudget Impact AnalysisQuality AssuranceData IntegrationStatement of Work GenerationContinuous Improvement
Soft Skills
Relationship BuildingOrganizational SkillsProblem-Solving SkillsVerbal CommunicationWritten Communication
Tools & Technologies
WindowsExcelWord
Industry Keywords
Clinical ResearchCentral Lab ServicesLife SciencePreclinical ResearchStudy Complexity Management
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 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 activities into databases and global monitoring plans
- Document and act on customer study-design requirements
- Perform quality self-reviews
- Participate in functional meetings and keep processes up to date
- Comply with the Central Lab Global Project Management strategy
- Manage a portfolio of global and local studies with varying complexities
- 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
- Master degree in a life science preferred
- 6 or more years experience in Central Lab Project management preferred
- 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
- Knowledge and experience in study design techniques related to creation and maintenance of protocol-specific databases and Statements of Work
- Ability to manage dynamic timelines, conflicting priorities, and varying study complexities
Benefits
Comp & perks- Equal Opportunity Employer commitment
- Consideration for qualified applicants without regard to protected characteristics
- Disability accommodations for online job searching and applications
- Access to an accessibility site or Labcorp Accessibility support
- Global career growth opportunities
- Opportunity to do meaningful work and make a real impact on people’s health