Sr. Manager, Early Clinical Development and Experimental Sciences

Tarrytown, New York, US
Nov 17, 2018
Required Education
Position Type
Full time
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases . Summary . Qualified physician or scientist with training in the pharmaceutical/biotechnology sector, or academic or clinical setting. Works closely with supervisor and other members of the cross-functional team, contributes to early development and clinical experimentation for projects for discovery phase through Proof of Concept POC . Job Duties . Supports the cross-functional study team on the following activities, including but not limited to . Collaborates on/designs POC-enabling human studies, First-In-Human FIH studies, POC clinical and/or pharmacologic studies and as per clinical strategy . Contributes to the medical and scientific portions of clinical study concepts CSCs and clinical study protocols CSPs and amendments . Identifies key internal and external collaborators/advisors . Conducts detailed literature reviews and analysis of development opportunities from mechanistic, pharmacological and clinical development perspectives . Defines hypothetical clinical benefit and risk . Contributes medical/scientific knowledge to timely and compliant clinical trial execution and quality of deliverables . Contributes to documents related to trials, monitoring plans, SAPs, amendments, IRB submissions and regulatory submissions . Analyzes, interprets and communicates clinical study data as needed . Contributes to collaborations with TFA Research and RGC to provide clinical and/or translational input to discovery targets/pipeline . Requirements . Education . Ph. D. degree, post-doctoral experience preferred, or . Bachelor's degree in biomedical subject, master's degree preferred, along with some industry experience . Experience . 0-3 years prior industry experience or clinical practice experience, preferably in a research/academic setting . Training in analysis of clinical and basic research information . Effective communications verbal & written and presentation skills are essential . Must be able to work productively in a fast-paced collaborative environment . Demonstrated/potential for critical thinking skills and sound decision-making . This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business . To all agencies . Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid . Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.