Job Information
Philips Associate Clinical Development Scientist in Shenzhen, China
Your role:
According to Clinical Evaluation process and regulations, guidelines
•Participate in the evidence generation processes for New Product introduction & Life-Cycle Management.
•Participate in the CDMA(Clinical Development and Market Access) process, develop 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.
About Philips
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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.