5 executive jobs found in New York, NY

We are seeking a Director to join our Clinical Development team. The Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Director leads in a matrix environment as part of a cross-functional team and may contribute to drug-candidate development projects through early and/or late phase development. The Director reports to the Internal Medicine Clinical Development Unit Lead of Clinical Scientists and collaborates closely with Medical Director(s)to provide scientific expertise vital to design and deliver on clinical studies and programs. As a Director, a typical day may include the following: May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist; Member of the Clinical Study Team and Global Clinical Sub Team Contributes to program team meetings,...

We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs. As an Associate Director a typical day may include the following: May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist Contributes to program team meetings, scientific advisory boards, study...

We are seeking an Associate Director within the Formulation Development Group of Regeneron Pharmaceutical Inc. at Tarrytown, NY. This role will lead clinical and commercial formulation and drug product development activities for peptides, monoclonal antibodies (mAb), antibody-drug conjugates (ADC), fixed dose combinations, and combination products. Specialized focus on obesity and metabolic disease. A typical day in this role might look like: Leads clinical and commercial formulation and drug product development activities for peptides, monoclonal antibodies (mAb), antibody-drug conjugates (ADC), fixed dose combinations, and combination products. Specialized focus on obesity and metabolic disease. Applies demonstrated knowledge of risk management and application of QbD principles to formulation and drug product development. Integrates analytical and process development. Interacts broadly and collaboratively with other Regeneron functions and stakeholders including...

Regeneron is seeking a Process Development Engineer I as a full-time position to work in the Purification Development group within Pre-Clinical Manufacturing and Process Development (PMPD). In this exciting role you will be primarily involved in the design and implementation of viral clearance studies to demonstrate virus safety of biotechnology products throughout the product development cycle from Phase I clinical trials through commercial licensure. A Typical Day in The Role Might Look Like: Design and leads multiple viral clearance projects with supervision Develops and qualifies scale-down models for viral inactivation, chromatography and membrane filtration unit operations Travels to external laboratories (20 – 25%) to execute viral clearance studies in accordance with GLP Collaborates with cross-functional groups to coordinate study logistics Summarizes studies and results in electronic laboratory notebooks, technical reports, and regulatory filings...

Regeneron Preclinical Manufacturing & Process Development group (PMPD), located in Tarrytown NY, is seeking a Process Development Engineer III for Plasmid Purification Process Development . In this role, you will work as part of a multi-functional team to develop Fermentation manufacturing processes, fermentation derived-starting materials, and products with the aim of providing treatment to unmet medical needs. A Typical Day in the Role Might Look Like: Leading the design, execution/optimization, scale-up and characterization of robust processes for purifying fermentation products (e.g., plasmid DNA and recombinant proteins) and starting materials from microbial expression platforms. Independently utilizing multivariate design of experiment approaches such as DOE with influences from experimental data and scientific literature to solve molecule specific-problems and optimize parameters for purification of fermentation starting materials and products. Designing and...