Director - Clinical Affairs - Ambry Genetics - Orange County

Job description
The Director of Clinical Affairs will function as a key player in Ambry’s clinical research programs, medical affairs, reimbursement and marketing functions.
She/he will be responsible for building a strong and effective Clinical Affairs Department and help direct the ongoing activities of medical communications and clinical study functions and provide support to medical marketing programs.
This individual will report directly to the CEO and will primarily participate in planning and implementing medical information and reimbursement activities, and will also provide support to the
Clinical Affairs field team.
In addition, this individual will help represent the company at professional advisory boards, KOL functions, collaborations with researchers and sales meetings.
The Director of Clinical Affairs will lead the strategy & implementation of obtaining insurance coverage for panel and exome testing.

Desired Skills and Experience
Essential Duties and Responsibilities:
Contribute scientific & clinical input to the new product development process.
Assist with scientific communications and marketing plans for product development.
Work closely with the Managed Care Department to provide clinical support to obtain coverage for Ambry’s panel and exome testing.
Support and present programs to educate customers about Client products, such as scientific publications, scientific presentations, etc.
Provide strategic and tactical input for the development of clinical trials, data collection, safety and medical information programs.
Write dossiers and economic analysis in support of panel testing and exome sequencing.
Education and Experience Requirements:
MS, CGC, PhD. Or MD, 6+ years of related clinical research and/or medical affairs experience

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