Remote Study Design Lead - Clinical Research

Labcorp; United States; À distance; USD 70 000 - 90 000; Plein temps

Avantages offerts par ce poste

Health benefits

401(k)

Stock Purchase Plan

Tuition reimbursement

Paid time off

Résumé du poste

Labcorp is seeking a remote Study Design Lead to join our Central Labs Services team. You will interpret sponsor protocol requirements and translate them into precise database designs that drive Statements of Work for CLS projects.

You will engage with external clients and partner with internal departments to evaluate feasibility and budget implications. Minimum qualifications include a high school diploma with 7+ years in clinical or preclinical research, and 1+ year of client exposure.

Qualifications

• Experience interpreting sponsor protocol requirements for study design.
• Ability to translate requirements into database design and SOWs.
• Strong client and stakeholder engagement throughout project lifecycle.
• Familiarity with clinical/preclinical research protocols and processes.
• Excellent verbal and written communication and relationship-building skills.

Responsabilités

• Interpret sponsor protocol requirements for CLS project database design.
• Deliver complete, accurate database designs with CLS feasibility.
• Engage with external clients across study design phases.
• Collaborate with internal teams to assess feasibility and budget impacts.
• Document client requirements and manage a diverse study portfolio.

Connaissances

Study design

Client engagement

Project coordination

Database design

Analytical mindset

Communication

Formation

Bachelor’s degree in life sciences

Description du poste

Labcorp is seeking a remote Study Design Lead to join our Central Labs Services team. You will interpret sponsor protocol requirements and translate them into precise database designs that drive Statements of Work for CLS projects.

You will engage with external clients and partner with internal departments to evaluate feasibility and budget implications. Minimum qualifications include a high school diploma with 7+ years in clinical or preclinical research, and 1+ year of client exposure.