Manager, Clinical Scientist, Hematology

Role Overview We are seeking a Manager in the Clinical Scientist, Hematology department. The Manager will lead the development, evaluation, planning, and execution of clinical studies and ensure scientific integrity and interpretation of study data for a clinical development program. The role reports to a Senior Manager, Associate Director, or Director, Clinical Sciences, and collaborates closely with the Medical Director to design and deliver clinical studies and programs. Location: Tarrytown, NY / Warren, NJ (Hybrid; 4 days per week on site). Responsibilities Member of the Clinical Study Team and Global Clinical sub‑team. Contribute to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings. Represent function in collaborative activities with other departments. Develop and maintain understanding of therapeutic disease areas and drug candidates, including biology, clinical manifestations, therapeutic standards, mechanisms of action, and drug landscape. Apply basic scientific expertise to support initiation and execution of clinical research for early and/or late‑stage assets. Assist in development of the Expanded Synopsis and author clinically relevant sections; review scientific portions of clinical trial protocols and amendments. Author and review documents related to trials, such as medical monitoring plans, SAPs, informed consents, and clinical components of the Clinical Study Reports; support development of regulatory documents; perform quality review. Maintain compliance with FDA, EMEA, ICH, and GCP guidelines and applicable SOPs regarding clinical safety. Prepare for external and stakeholder meetings (IM, Governance, DMCs, Regulatory Authority). Present data and information to external investigators (SIV) and internal collaborators. Influence within the team and across functional areas; exhibit strong analytical, presenting, and communication skills. Qualifications Bachelor’s degree required; advanced degree or equivalent in life science/healthcare preferred (PhD/MD/PharmD/MSc). Minimum 3 years of pharmaceutical clinical drug development experience. Basic knowledge of oncology or hematology therapeutic areas and a proven track record in clinical trial process improvements. Proven leadership and accomplishments in all aspects of conducting global clinical trials and executing clinical programs. Proficient knowledge of clinical development process, regulatory requirements, and ICH/GCP guidelines. Ability to resolve novel problems requiring creative application of advanced skill, training, and education. Benefits Regeneron provides comprehensive benefits that vary by location, including health, dental, vision, life, and disability insurance; fitness center access; 401(k) with company match; family support benefits; equity awards; annual bonuses; paid time off and paid leaves (including military and parental leave) for eligible employees at all levels. Salary Range (annually): $128,600.00 – $210,000.00. EEO Statement Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief, 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. #J-18808-Ljbffr