Sr Director, Clinical Development (MD)

Start free →

Or apply yourself on the official page →

About the role

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Job Description The Senior Medical Director provides clinical oversight to one or more clinical trials. Additionally, the Senior Director guides the project teams to design and implement clinical studies at high quality and in a time and cost-effective manner in line with the department and corporate goals and within regulatory and resource guidelines.   Job Responsibilities • Provide clinical oversight and medical monitoring to one or more clinical trials • Lead project teams to design and implement clinical studies • Write protocols, investigator brochures, clinical study reports and review clinical trial documents • Conduct investigator meetings and lead site initiation visits with clinical trial investigators • Implement and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets • Translate findings from research and nonclinical studies into clinical development opportunities • Interact with clinical investigators and thought leaders • Work with internal regulatory affairs team and other ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines • Work with internal pre-clinical scientists, translational scientists, business and commercial organizations in a cross functional manner • Work in a team environment comprising clinical operations, biomarker specialists, CROs, and regulatory affairs • Provide clinical expertise and input for regulatory filings (i.e., BLA, MAA) as well as response to questions from regulatory authorities in the context of IND submissions, clinical trial applications or filing procedures • Provide clinical guidance and work in a team environment in interactions with external stakeholders (medical experts, advisory boards, patient advocacy groups) and internal stakeholders (Research, Translational Sciences, Clinical Operations, Safety, Regulatory, Medical Affairs, and Commercial) • May present scientific information at scientific conferences as well as clinical study investigator meetings. Where applicable, takes a lead on authoring scientific publications • May assist in the clinical evaluation of business development opportunities   Basic Qualifications MD/DO and 6+ years of clinical research or drug development experience Preferred Qualifications • Board certification/specialization in neurology and experience managing phase 1-3 trials; late stage experience is preferred • 4+ years of relevant drug development experience, either within industry or as a clinical investigator/physician scientist in academia, or equivalent experience; drug development experience in neurological diseases including neuro autoimmune diseases are highly desired • Demonstrated clinical development strategist with experience designing, implementing and conducting clinical trials, with emphasis on proof-of-concept and first-in-human studies • Stra

View the official posting →