Role OverviewThe Study Design Lead will interpret sponsor protocol requirements and translate them into a precise, study-specific database design. They will apply deep technical, therapeutic area, client, and CLS process knowledge to deliver a complete and accurate database design for the CLS project. The role involves regular engagement with external clients throughout all phases of study design and development, as well as partnering with internal departments to understand full organizational capabilities and evaluate feasibility of client requests related to study design.
What You Will Do
The Study Design Lead will serve as a consultant on study design decisions, collaborating with the Global Study Manager (GSM) to identify risks and budget implications. They will also coordinate internal processes and communications, including feasibility assessments, material transfer agreements, and supply forecasting, and ensure all follow-up actions are incorporated into the database and global monitoring plan.
Why It Might Be a Fit
The Study Design Lead will have the opportunity to do meaningful work, grow their career, and make a real impact on people's health around the world. They will be part of a global contract research organization within Labcorp, offering a common set of processes, procedures, and instrumentation across sites in Europe, Asia/Pacific, and the United States.
Requirements
- 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
Benefits
- Medical
- Dental
- Vision
- Life
- STD/LTD
- 401(k)
- Paid Time Off (PTO) or Flexible Time Off (FTO)
- Tuition Reimbursement
- Employee Stock Purchase Plan
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