Associate Medical Director, Clinical Development - Job ID: 1912, 1913, 1914

- Leverage medical expertise and hands-on clinical experience to promote relevance and rigor of the development program - For clinical trials: design, provide medical oversight, and support site and subject retention - Serve as a Medical Monitor for clinical trials, ensure study integrity, and track accumulating safety and efficacy data - Provide leadership to study teams - Ensure successful completion of trial-related documents (including clinical trial protocols, investigator brochures, medical monitoring plans, site training materials, clinical study reports, health authority responses, standard operating procedures, etc.) with cross-functional team members - Anticipate obstacles within a clinical trial, and implement solutions - Analyze, evaluate, interpret, and report study results - Contribute to drafting and reviewing clinical documents, manuscripts, presentations, and regulatory submissions - Contribute to design of the Clinical Development Plan - Maintain up-to-date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance - Collaborate with-and serve as a clinical research resource for-cross-functional colleagues to optimize product development - Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders to represent the interests of the company - Contribute to corporate strategic and organizational initiatives - Assist with commercial activities as needed - Complete assigned tasks thoroughly, accurately, and on time - Adhere to rigorous ethical standards - Travel up to 20% domestically and internationally for scientific meetings

- M.D. degree - Completion of ACGME-accredited residency and fellowship (strongly preferred) - Physician licensure in at least one state (strongly preferred) - Board-certified (strongly preferred), with specialty in endocrinology highly desired - At least 3 years of industry (other relevant experience e.g. post-graduate experience in the clinical and/or academic realms may also be considered on a case-by-case basis). - At least 2 years of experience with clinical trial design and execution - Strong track record of scientific and clinical inquiry - Possess excellent communication skills (written and oral) - Learn quickly, follow complex directions under pressure - Multi-task while remaining organized and attentive to detail - Lead both directly and by example - Work hard, be a trustworthy and collaborative team player - Take initiative and solve complex problems - Demonstrate sound judgement in terms of handling complex, confidential, and regulated information

The estimated salary range for this position is $255-265K/year. Actual salary determination is dependent on a variety of factors some of which include: experience, qualifications, and geographic location. This position may be eligible for a discretionary annual bonus or an incentive compensation plan (eligibility varies based on role and position level), discretionary stock-based long-term incentives, paid time off, and a comprehensive benefits package.