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Associate director hematology

Cerus Corporation

This is a Full-time position in Concord, CA posted October 6, 2019.

& of :Lead development studies to support the INTERCEPT Platelet and Plasma platforms with focus on registration studies with external collaborators. Be a technical expert and key member of the Development team in the areas of plasma. Primary :
· Manage laboratory team to support registration studies to meet corporate timelines.
· Interface with cross functional team leaders at Cerus.
· May act as Study Director or Principal Investigator for internal or external Cerus registration studies.
· Reduce and analyze highly complex data and present it to maximize clarity and impact.
· Serve as a technical expert on project teams, including contribution of ideas, development and execution of plans, and timely reporting of the results.
· Serve as technical expert on external collaborations and studies; including meeting with customers and other external parties as a representative of the company in area of expertise.
· Work cross functionally with Clinical, Regulatory, Quality and Biostatistics departments.
· Write protocols and study reports.
· Maintain leading edge knowledge in primary field of expertise.
· Maintain high level of professional expertise through familiarity with scientific literature and attendance at scientific meetings.
· Write and submit abstracts to national and international conferences.
· Present internally and at scientific conferences and contribute to scientific publications.
· Support regulatory submissions to global health authorities.
· Supervise, manage, and/or provide guidance to other personnel.
· Train and mentor research associates, assistant scientists or scientists.
· Identify patentable inventions.
· Perform other related duties and support other projects as required.

with a minimum of 7 years relevant experience or Master’s degree in a scientific discipline with a minimum of 10 years of experience.
· Excellent communication skills with the ability to interface at all levels including management (encompasses verbal, written, interpersonal, listening)
· Working knowledge of blood bank practices.
· Familiarity with GLP/GMP regulations & record keeping.
· Ability and presence to interface effectively at all levels; including customers, business partners, management and employees globally.
· Ability to work on complex problems in which analysis is required to determine appropriate course.
· Proficient in writing reports, regulatory submissions and publications.
· Solid experience with related computer software.