Medical Director, Hemophilia

Highly Competitive Salary
  1. Permanent
  2. Director, VP & Physician
  3. United States
San Rafael, California
Posting date: 01 May 2019
ME.AG.22970_1556739301

ProClinical, in support of our client, are seeking an individual to fill the role of Medical Director of Hemophilia, based in San Rafael, CA. The successful candidate will be a critical strategic and execution focused individual in the Medical Sciences function, leading North American Regional Medical Affairs activities from pipeline through post approval status.

Responsibilities

  • Develop and communicate Global Medical Plan in collaboration with Medical Affairs stakeholders.
  • Act as an expert and primary contact point for all global compound or disease area related issues.
  • Identify, develop and maintain the scientific messaging platform.
  • Conduct critical appraisal of available scientific and medical knowledge, identify gaps and identify and lead activities to address deficiencies.
  • Review and approve all product materials.
  • Drive scientific messaging and gap analysis as well as communications.
  • Contribute to the development of, and review and approve global publication plans.
  • Act as the Medical Affairs representative on key product and development strategic focused teams.
  • Lead the Medical Affairs product team and represent Medical Affairs on relevant commercial teams.
  • Market relationship and access development.
  • Ensure appropriate access to key opinion leaders during entire product lifecycle.
  • Provide oversight for international symposiums, advisory boards and manuscripts.
  • Develop Medical Affairs product launch strategy and roadmap.
  • Lead all launch activities in collaboration with Commercial and other key stakeholders
  • Assist in writing medical need, natural history and risk/benefit sections of BLA and MAA.
  • Lead development/design and monitoring of PMC/PMRs and other relevant studies.
  • Assist in critically evaluating study results in statistical and final reports and ongoing reviews with study investigators.
  • Conduct critical scientific and medical review of IR protocols.
  • Design studies and develop protocols in a wide range of types of study phases pre and post marketing.
  • Support early disease training across the company.

Skills and Qualifications

  • MD with US licensure or fellowship required; BS in life or health sciences.
  • 2+ years of industry experience in hemophilia or genetics; 5+ years of relevant experience in clinical science, medical affairs, and/or drug development preferred.
  • Demonstrate deep medical and scientific knowledge for key therapeutic areas
  • Demonstrate solid understanding of cross-functional interdependencies across the drug development life cycle.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Anna Graham at (+1) 415-660-4945 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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