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of post-doc experience in the relevant field . Successful record of scientific accomplishments as indicated by scientific publications and presentations. Demonstrated ability to review critically available
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Lead and contribute to internal communications regarding pre- and post-congress coverage reporting Manage agencies and offshore teams to ensure medical content development aligned with global medical
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biology or related field with established advanced capability and track record in developing and applying computational and bioinformatics methods. Five years or more of post-PhD academic and/or industry
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Lead and contribute to internal communications regarding pre- and post-congress coverage reporting Manage agencies and offshore teams to ensure medical content development aligned with global medical
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This posting covers two available positions (I&I and Rare Disease). Therapy area responsibility will be determined through the selection process. ROLE SUMMARY Specialty Care (SC) Medical Affairs
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disease states to optimize doses, dosage regimens and study designs throughout all phases (first-in-human through post-approval) of clinical drug development. With guidance, identify opportunities where
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sections during Lead Development stage preparing for IND submission post Candidate Selection (CS). You and your team will author the nonclinical pharmacology modules of all regulatory submission documents
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(s) assigned could be in development and/or at post-authorization stage. How You Will Achieve It Responsible for the production, updating and communication of global regulatory strategies for assigned
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This posting covers two available positions (I&I and Rare Disease). Therapy area responsibility will be determined through the selection process. ROLE SUMMARY Specialty Care (SC) Medical Affairs
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development to support launch and post-launch success. BASIC QUALIFICATIONS Clinically trained (MD, ClinPharm), PharmD, MD-PhD desired Oncology medical professional with strong experience (at least 9 years if