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Your role:
According to Clinical Evaluation process and regulations, guidelines
Participate in the CDMA(Clinical Development and Market Access) process,velop clinical and health economic evidence to support market authorization, market access and market adoption.
Participate in the development of clinical deliverables, including clinical evaluation plans and reports, clinical trial protocols and reports, PMCF plans and reports & clinical sections of regulatory submissions
Work closely with Clin Ops and BS&DM on day to day management of assigned clinical studies
Support clinical literature searches and reviews.
You're the right fit if:(4 x bullets max)
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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