Director Medical Affairs, Pharma Services

Job title: Director Medical Affairs, Pharma Services

Company:

Job description: The position
Join an experienced, cohesive and collaborative international Medical Affairs team of dedicated professionals from diverse backgrounds. This is an unparalleled opportunity for personal career development and ongoing job satisfaction as you enable advances in Personalized Healthcare around the globe. Work with the Leading Pharmaceutical / Biotech Company Sequencing Solutions (RSS) Disease Area Lifecycle Team to support commercialization of Oncology CLIA testing services for pharma/biotech partners. The position is based in San Jose, CA and/or Pleasanton, CA, USA.

Essential Functions of your Director Medical Affairs, Pharma Services role include the following:

Represent Medical Affairs providing medical leadership and clinical expertise in interactions with pharma/biotech partners as well as RSS Commercial and Marketing, Business Development, Clinical Operations, Regulatory, Quality, R&D, Bioinformatics and other functional groups as needed
Serve as a subject matter expert in genetic testing in Oncology and Personalized Healthcare
Develop and execute the medical plan for RSS’ Oncology CLIA testing services
Respond to medical questions from pharma/biotech partners, healthcare providers and other established as well as prospective clients
Support cross-functional project teams responsible for the development, validation and commercialization of RSS’ Oncology CLIA testing services
Analyze medical and scientific literature, clinical outcomes of published studies and effectively communicate knowledge within and outside the organization
Train internal colleagues, field teams, speakers and established as well as prospective clients either live or by webinar
Develop, review and update scientific and clinical content for current product and product extensions including website, brochures, test reports and training and presentation materials
Attend key scientific congresses to provide on-site support and report back key insights through conference reports
Plan and execute on scientific symposia and educational events at key internal meetings and international scientific congresses, including managing speakers
Organize and run scientific advisory boards
Design, implement and report non-registrational clinical trials and manage investigator initiated studies
Prepare abstracts, posters and presentations for regional, national and international meetings
Write manuscripts for publication
Evaluate and support the development of SOPs
Supervise and/or mentor others as needed

Who you are
You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.
You have an MD (preferred) and/or PhD with at least 6 years of industry experience in medical affairs and/or clinical development or other relevant practice experience. Along with the following skills:

Capability to provide subject matter expertise in Oncology and Personalized Healthcare
Understanding of legal and regulatory considerations impacting pharma/biotech industry
Clinical and/or laboratory experience in Oncology (e.g. board-certification in Oncology) preferred
Experience with clinical trials
Ability to develop relationships with current and prospective clients
International experience, working in a cross-cultural environment
Excellent oral and written communication skills
Willingness to travel up to 30% nationally or internationally

Expected salary:

Location: Pleasanton, CA

Job date: Wed, 16 Dec 2020 23:50:07 GMT

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