Backed by NEA.
About the role
• Contribute to data management activities in support of clinical studies, including: o eCRF development by leading cross-functional reviews of eCRF content.
What they're looking for
- • BS/BA in scientific discipline, MS or equivalent preferred, with at least 8 years related experience in
- a CRO/pharmaceutical/biologics/biotechnology company
- • Study/Vendor oversight experience
- • Experience with global studies, utilizing an outsourced CRO model
- • Expert knowledge of Data Management processes, efficient design/build of an EDC data
- management system and other Clinical Trial/Data Management Systems
More about this role
Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
The Lead Clinical Data Manager will contribute and lead data management activities in support of client
studies across all stages of clinical drug development. They will be responsible for working with cross
functional teams leading the data management initiatives.
The ideal candidate has experience working in a global CRO setting with an excellent understanding of
data management best practices, good clinical practice, and applicable regulatory requirements. This
candidate will have direct experience developing a data management department. Experience with all
phases of clinical trials, with strong oncology and phase 1 experience, is critical.
• Contribute to data management activities in support of clinical studies, including:
o eCRF development...
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