Sr. Development Scientist myoscience
THIS JOB HAS EXPIRED Note: The following is meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title.
-- Translate corporate strategy and market development priorities into a comprehensive research program. Conduct research program in support of corporate goals and commercial initiatives.
-- Define and conduct pre-clinical studies to study and gain a thorough understanding for aspects of Focused Cold Therapy of the nerve.
-- Develop bench-top methods for evaluating the performance and dose of Focused Cold Therapy devices targeting different indications. Validate these measurement methods with pre-clinical or clinical experiments.
-- Develop simulation models to predict device performance and streamline prototype development. Validate simulation tools with experimental data.
-- Publish myoscience research reinforcing myoscience as the preeminent cold treatment of the nerve for aesthetic and therapeutic indications.
-- Direct involvement in Scientific Advisory Board meetings, Science & Technology BOD meetings, focus groups, and KOL relationships with myoscience.
-- Evaluate electrical nerve stimulation devices and methods to provide guidance for the myoscience treatment.
-- Develop and lead a world-class research organization within and extending outside of myoscience through research collaborations.
-- Evaluate new opportunities with an emphasis on science, IP, and technology; provide recommendations towards M&A activities.
-- Transfer research knowledge into product development, clinical affairs and marketing in support of technology, product and treatment development.
-- Stay up-to-date and follow all procedures related to this job that can affect the quality of products or services provided to our customers.
Experience, Education, Training, Traits:
-- BS or MS plus seven years experience or its equivalent in pharmaceutical or medical devices. At least 2 years experience direct employee management/supervision or its equivalent.
-- Proven track record of employee management or supervision.
-- Proven track record of effective medical research and publishing.
-- Working knowledge of project planning and management including use of PM software such as MS Project.
-- Experience in representing research portfolio to investors, strategic interests and regulatory bodies.
-- Experience applying research results in the preparation of 510k or PMA regulatory submissions seeking medical device clearance in new indications.
-- Ability to read, analyze, and interpret engineering specifications, general business periodicals, professional journals, technical procedures, or government regulations.
-- Ability to write reports, specifications, business correspondence, and procedure manuals.
-- Ability to effectively present information and respond to questions from groups of managers, investors, clients, customers, and the general public.
-- Ability to clearly and concisely convey project accomplishments, obstacles, issues and status to project team members.
-- Ability to define problems, design experiments, collect data, establish facts, analyze data and draw valid conclusions.
-- Strong team-working and communication skills. A drive to get the job done in the face of obstacles and time constraints, and a willingness to jump in wherever needed.
THIS JOB HAS EXPIRED