Medical Director, Clinical Development - Job ID: 1930

• →Contribute to formulation and implementation of the Clinical Development Plan

• →Leverage medical expertise and hands-on clinical experience to promote relevance and rigor of the development program
• →For clinical trials: design, provide overall 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 teams of medical monitors
• →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
• →Ensure study integrity, and track accumulating safety and efficacy data
• →Analyze, evaluate, interpret, and report clinical data
• →Anticipate and solve complex drug development problems
• →Contribute to regulatory strategy
• →Contribute to drafting and reviewing of clinical documents, manuscripts, presentations, and regulatory submissions
• →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 (e.g. in clinical operations, statistics, regulatory affairs, medical affairs, health economics outcomes research, commercial, finance) to optimize product development
• →Contribute to (and may be asked to represent the clinical development department in) corporate strategic and organizational initiatives
• →Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders to represent the interests of the company
• →Assist in portfolio management and 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 5 years of industry experience (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). Those with less experience may be considered for an Associate Medical Director position.
• At least 3 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 $265-295K/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.