About this opportunity
Regeneron Pharmaceuticals, Inc (USA) lists this Associate Director, Clinical Scientist, Cardiovascular/Metabolic disease opportunity in village of tarrytown, New York. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Clinical Sciences (Internal Medicine) to join our Clinical Sciences team, supporting our global clinical development programs in cardiovascular, renal, and metabolic disease. In this role, you will lead the design, execution, and scientific interpretation of clinical studies, ensuring data integrity and patient safety while partnering closely with Medical Directors and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
Location: Tarrytown, NY, Warren, NJ, Cambridge, MA
Work model/flexibility: Primarily on-site with hybrid flexibility
Discover your role
Lead clinical studies and programs in a matrix environment, serving as lead Clinical Scientist or delegate for the therapeutic area
Partner with Medical Directors to deliver the scientific expertise needed to design and complete early and/or late-phase studies
Develop expanded synopses and author or review protocols, amendments, medical monitoring plans, SAPs, informed consents, and clinical study report sections
Propose and communicate study strategies grounded in the supporting literature and a deep understanding of the disease area, mechanism of action, and drug landscape
Present data and plans to investigators, governance bodies, DMCs, and regulatory authorities, and contribute to advisory boards and steering committees
Perform clinical and medical data review, including safety monitoring, to protect patient safety while upholding FDA, EMA, ICH, and GCP standards
Identify risks, design mitigation strategies, and promote consistent data review practices across studies and programs
Mentor and coach junior team members and cross-functional colleagues
This role requires
MS/PhD/PharmD in a related field with 10+ years of pharmaceutical clinical drug development experience (other levels considered depending on experience)
Experience managing clinical trials in one or more of the following therapeutic areas: cardiovascular, renal, or metabolic disease
Proficient knowledge of the drug development process, GCP, ICH guidelines, study design, and clinical research methodology
Solid medical writing skills, with the ability to communicate clear, concise messages and present with confidence
Demonstrated leadership in conducting global clinical trials and executing clinical programs
Proven ability to influence cross-functionally, resolve novel problems creatively, and drive clinical trial process improvements
Salary Range
$176,100.00 - $287,300.00
Regeneron is committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role:
annual bonuses or other incentive plans
equity awards
pension or retirement benefits
401(k) company match
health and wellness programs
fitness centers
insurance benefits (e.g. medical, dental, vision, life and disability)
paid time off
family support benefits
For jobs in Canada: this posting is for an existing position.
Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.
#J-18808-Ljbffr
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.