Study Design Lead - Ff190

Join our talent Pool for future needs!!! Get ready to redefine what's possible and discover your extraordinary potential . Here at Labcorp Drug Development, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose , you'll be empowered to own your career journey with mentoring, training, and personalized development planning. Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients—and your career.
The Position This position falls within our Central Labs Services group supporting Central Labs Projects for clinical trials phases I-IV. This position is remotely based. 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. In this position, you will be responsible for the following:
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 Labcorp 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.
Do you have the following education and experience? Bachelor of Science degree (flexible to consider those without a degree that have significant related experience).
Minimum of 3 years of study design experience (can include clinical database design).
Minimum of 2 years of experience interpreting and translating clinical research protocols.
Technical writing experience is desirable.
Experience managing clinical trial projects is a plus.
Labcorp is proud to be an Equal Opportunity Employer : As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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