
Study Design Lead
As a Study Design Lead, you will collaborate with our pharmaceutical company clients to review clinical protocols, define the components of clinical trial study designs, and work with internal teams to highlight risks and financial impacts associated with various study design options. Accurately interpreting clinical protocol requirements and coordinating the preparation of Covance clinical trial databases. Utilizing technical, therapeutic area, and pharmaceutical industry knowledge to successfully coordinate the completion of Covance clinical trial databases. Coordinating internal processes and communications related to study design and ensuring that follow-up actions are recorded and global monitoring plans are implemented. Ensuring that all customer requirements are documented and acted upon. Building strong relationships to ensure high quality study design.
Minimum of 3 years of study design experience (can include clinical database design)
Minimum of 2 years of experience interpreting and translating clinical protocols
Documentation
Time Management
Presentation skills
Technical writing skills
Multitasking
Process Improvement
Detail Oriented
Communication Skills
Problem-Solving
According to JobzMall, the average salary range for a Study Design Lead in 4307 Emperor Blvd, Durham, NC 27703, USA is $107,000 to $130,000 per year. The salary range can vary depending on experience, qualifications, and other factors.
Apply with Video Cover Letter Add a warm greeting to your application and stand out!
Covance Inc. is a contract research organization headquartered in Princeton, New Jersey, providing nonclinical, preclinical, clinical and commercialization services to pharmaceutical and biotechnology industries. The company is owned by LabCorp and employs more than 50,000 people in over 60 countries. In 2014, Laboratory Corporation of America- Labcorp, purchased Covance.

Get interviewed today!
JobzMall is the world‘ s largest video talent marketplace.It‘s ultrafast, fun, and human.
Get Started