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Philips Associate Clinical Development Scientist China, Guangdong Province, Bao'an District 74951741
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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)
- Education: Master or PhD in clinical medicine;
- Medical Experience: Cardiology, Anesthesiology, Emergency Medine, Critical Care Medicine Experience.
- Experience:1-3 years’ experience in clinical development function or related clinical area;
- Competencies and Skills:
- Demonstrated expertise in NMPA and/or MDR regulatory requirements and clinical data interpretation;
- Effective organizing, communication, and project management skills; ffetive verbal and written skills in both English and Mandarin;
- Proficient in Biostatistics software is preferred.
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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