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The Temp Associate Director, Global Trial Optimization (GTO) is responsible for providing strategic insights, expert recommendations, tailored training content, and specialized deliverables in support of the GTO leadership team’s core process areas (strategic feasibility, site identification, patient engagement, and enrollment planning).We expect the Associate Director to demonstrate their advanced feasibility knowledge and extensive experience, and involve collaborating with leaders and internal collaborators to drive new GTO process development and optimize current strategies. We believe the A/D will lead and provide expert guidance to ensure operational excellence and consistent, effective, high-quality project delivery through development of the onboarding process of new team members and the ongoing training and support of current team members. The role reports into the Head of Global Trial Optimization.In this role, a typical day might include:
Provides leadership input and expertise in support of GTO team’s generation of consistent, high-quality, and timely insights to inform study design, study placement, operational planning, and patient and site engagement strategies
Partners with GTO Head and capability process leads, providing expert insights and recommendations into the development of GTO strategy & process, ensuring that expectations for key GTO deliverables are met.
Contributes as a Subject Matter Expert to the development and implementation of core GTO functions, processes, and procedures, as well as cross-functional and organizational process improvement initiatives as required.
Uses company and department-level experience and strategic analysis to develop and drive viable, enduring solutions to optimize strategic feasibility and patient engagement delivery
This role might be for you if have:
Extensive experience in global clinical trial operations required
Compelling communicator with ability to deliver accessible scientific and technical information to a variety of audiences
Proven ability to lead teams and build strong internal and external working relationships in a diverse range of environments
Experience in leading activities and providing strategic input that aligns with clinical development plans (CDPs)
To be considered for this opportunity, we expect you to have at least 8 years of trial optimization experience within a sponsor or CRO environment. We also require the AD to have a bachelor's degree at a minimum.Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
