Labcorp Drug Development Job - 40042635 | CareerArc
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Company: Labcorp Drug Development
Location: Geneva, GE, Switzerland
Career Level: Associate
Industries: Healthcare, Pharmaceutical, Biotech

Description

Job Overview:

This position falls within our Central Labs Services group supporting Central Labs Projects for clinical trials phases I-IV. This position is remotely based anywhere in the US.

 

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 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

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
Education/Qualifications:
  • Bachelor's degree 
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

A combination of education, training, and experience may be considered.


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