Global Study Design Lead, Client-Facing & Strategy

Labcorp; Indianapolis (IN); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(k)

PTO or FTO

Tuition Reimbursement

Employee Stock Purchase Plan

Job summary

Labcorp seeks a highly experienced database design consultant to translate sponsor requirements into precise study-specific designs for CLS projects. You will work with clients and internal teams to ensure feasible, robust study designs and quality processes across global trials.

With 7+ years in clinical or preclinical research and strong communication, you will guide decision-making, mitigate risks, and manage diverse study portfolios in a collaborative environment.

Qualifications

• 7+ years of professional experience in clinical or preclinical research.
• 1+ years of experience working directly with clients and stakeholders.
• Strong scientific acumen and investigative mindset.
• Excellent verbal and written communication skills.

Responsibilities

• Interpret sponsor protocol requirements and translate them into a precise study-specific database design for CLS projects.
• Apply deep technical, therapeutic area, client, and CLS process knowledge for complete database designs.
• Engage regularly with external clients through all study design phases.
• Partner with internal departments to evaluate feasibility of client requests in study design.
• Consult on study design decisions with GSM, identifying risks and budget implications.
• Coordinate feasibility assessments, material transfer agreements, and supply forecasting; document actions.
• Document all client requirements related to study design.
• Manage a diverse portfolio of global and local studies with varying complexity.

Skills

Client relationship management

Verbal & written communication

Analytical mindset

Relationship-building

Self-motivation

Education

Bachelor’s degree in life sciences

Job description

Labcorp seeks a highly experienced database design consultant to translate sponsor requirements into precise study-specific designs for CLS projects. You will work with clients and internal teams to ensure feasible, robust study designs and quality processes across global trials.

With 7+ years in clinical or preclinical research and strong communication, you will guide decision-making, mitigate risks, and manage diverse study portfolios in a collaborative environment.