Strong product management background (i.e., experience writing and grooming technical user stories, working with Design and engineering teams to formulate and delivery experiences to market) Sound understanding of engineering and systems Good business acumen to understand how products are commercialized Understanding of analytics (how to identify what data is needed to determine effectiveness of experience, understanding of customer research, etc.) Experience in Sales and Service is a plus
EDUCATION/CERTIFICATIONS:
Bachelor's degree or four or more years of work experience.
The Clinical Study Associate Manager (CSAM) role supports the Clinical Study Lead by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance of direct execution versus oversight of CROs deliverables will vary accordingly. You will work with the study team internally and externally with vendors such as CROs in feasibility, planning, initiation, maintenance and closeout of clinical projects according to GCP, ICH, CFR and Regeneron Standard Operating Procedures (SOPs). Travel to study sites may be required to assist with monitoring clinical studies.
