Regeneron Pharmaceuticals

TheTempClinical Study Specialist (CSS)provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The Temp CSS may be assigned to support the execution of one or more studies across a program. The Temp CSS receives assignment More...

The Executive Medical Director Clinical Sciences Obesity is responsible for effectively executing large and/or complex studies and/or programs and serves as an expert resource to anticipate/resolve study/asset clinical and conduct issues. For assigned programs the incumbent will serve More...

As a Senior Manager Technical Product Manager you will apply your Workday HCM technical solutions capabilities and systems/software expertise support our global employee base. We work on HCM product design technical solutions and integration of the product/software being implemented. More...

This role is onsite 4 days week and 1 day from home. The Director Program Operations Leader (POL) is responsible for leadership and overall strategic management of one or more complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations a More...

Associate Manager Clinical Data Management (CDM) collaborates with vendor Project Managers and Clinical Data Managers to ensure Data Management functions comply with regulations and study protocols. This role involves preparing the Data Management Plan (DMP) according to company SOPs More...

We are looking for a highly motivated Principal Scientist Clinical Pharmacology in our Pharmacometrics (PMx) group. The position will report to the Senior Group Director (SGD) within Clinical Pharmacology (CP) in the General Medicine (GM) group. You will represent CP on project teams More...

We are seeking a dynamic and analytical Manager for our Commercial Operations team in Munich Germany. This pivotal role supports strategic and tactical decisionmaking in marketing and sales focusing on the Immunology & Inflammatory Teams across Germany Switzerland and Austria. As More...

In this role you will have responsibility for reporting and managing data related to Trade performance in global markets outside of the U.S. You will manage data from multiple 3PLs wholesalers and distributors along with internal supply chain information to measure inventory turns DOH More...

A principal statistical programmer provides timely support to the study team on all programming matters according to theproject strategies. As an integral part of a study the incumbent provides project leadership and programming support forprocessing data from clinical studies. Requir More...

We are seeking a highly motivated Senior Manager Business Operations Cost Management who will be responsible for cost management activities regarding running clinical trials. The Senior Manager Business Operations Cost Management will work at the portfolio program and functional level More...

We are seeking a Principal Scientist with a focus in Neurology and/or Ophthalmology to join our Clinical Imaging team. Youwill conceptualize support execute operationalize and optimize complex early to latephase clinical trials where imaging plays a central role. Work closely with Reg More...

This role is onsite 4 days per week and 1 day from home. A fully remote role is not possible. The Director Program Operations Leader (POL) is responsible for leadership and overall strategic management of one or more complex programs in Clinical Trial Management (CTM). This individual More...

The Associate Director Precision Medicine Clinical Laboratory Operations will be responsible for Clinical Laboratory Project & Program management for various therapeutic areas working closely with Director Precision Medicine Clinical Laboratory Operations and key crossfunctional c More...

The Senior Manager Data Management provides Clinical Data Management oversight to Data Managers and Associates to ensure CROs and vendors are performing in compliance with Regeneron procedures. Ensure consistent processes across all studies for multiple projects or TA. Provides coachi More...

The Senior Manager Data Management provides Clinical Data Management oversight to Data Managers and Associates to ensure CROs and vendors are performing in compliance with Regeneron procedures. Ensure consistent processes across all studies for multiple projects or TA. Provides coachi More...

We are seeking an experienced and motivated Principal Scientist to support cell therapy target ID and validation and CART/TCR preclinical research as a part of Regeneron Cell Medicines (RCM). You will be responsible for the identification and validation of novel targets for CAR T cell More...

The Senior Manager Clinical Study Lead (CSL) is expected to operate with highdegree of independence and is accountable for the global of assigned large and/or complex clinical trials from study design through to study close out. The Senior CSL is accountable for the study timelines More...

The Manager Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality preclinical and clinical areas of drug development and the policies More...

This is a hybrid position that requires 3 nonconsecutive days onsite in Armonk NY or Basking Ridge NJ and 2 days from home. A fully remote role is not possible for this position.The Associate Director Strategic Facilitation will objectively lead discussions or workshops ensuring busin More...

The Senior Director Precision Medicine Biomarker Lead Solid Tumor role is critical for the successful of Regeneron biomarker strategies. Will be accountable for leading a team responsible for overseeing the development and of biomarker strategies for the burgeoning Oncology Portfol More...