Study Design Lead , Central Lab Services - Clinical Research

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 10pt;">This position falls within our Central Labs Services group supporting Central Labs Projects for clinical trials phases I-IV. This position is remotely based.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 10pt;">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:</span></p><ul><li><span style="font-size: 10pt;">Accurately interpreting clinical protocol requirements and coordinating the preparation of Covance clinical trial databases</span></li><li><span style="font-size: 10pt;">Utilizing technical, therapeutic area, and pharmaceutical industry knowledge to successfully coordinate the completion of Labcorp clinical trial databases</span></li><li><span style="font-size: 10pt;">Coordinating internal processes and communications related to study design and ensuring that follow-up actions are recorded and global monitoring plans are implemented</span></li><li><span style="font-size: 10pt;">Ensuring that all customer requirements are documented and acted upon</span></li><li><span style="font-size: 10pt;">Building strong relationships to ensure high quality study design</span></li></ul><p style="margin: 0px;"><span style="font-size: 10pt;">Do you have the following education and experience?</span></p><ul><li><span style="font-size: 10pt;">Bachelor of Science degree (flexible to consider those without a degree that have significant related experience)</span></li><li><span style="font-size: 10pt;">Minimum of 3 years of study design experience (can include clinical database design)</span></li><li><span style="font-size: 10pt;">Minimum of 2 years of experience interpreting and translating clinical research protocols</span></li><li><span style="font-size: 10pt;">Technical writing experience is desirable</span></li><li><span style="font-size: 10pt;">Experience managing clinical trial projects is a plus</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10pt;">Bachelor's degree </span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10pt;">Minimum of 3 years of study design experience (can include clinical database design)</span></li><li><span style="font-size: 10pt;">Minimum of 2 years of experience interpreting and translating clinical research protocols</span></li><li><span style="font-size: 10pt;">Technical writing experience is desirable</span></li><li><span style="font-size: 10pt;">Experience managing clinical trial projects is a plus</span></li></ul><p style="margin: 0px;"><span style="font-size: 10pt;">A combination of education, training, and experience may be considered.</span></p>