Regeneron Pharmaceuticals

The AD Program Manager is responsible for driving strategic and complex cross-functional transformation programs aimed to streamline and influence the drug development process across R&D. The programs being led by the AD Program Manager consist of interconnected projects that are المزيد...

Regeneron is seeking a seasoned highly motivated Technical Product Manager with HCM technical solutions capabilities and systems/software expertise to support both US / ex-US countries. This position requires skills in HCM product design technical solutions in depth technical knowledg المزيد...

As a Senior Director of IT Quality Assurance and Compliance you will lead a team of those managing 20 to 30 members The focus is to provide leadership coaching and technical support to the IT QA & Compliance Management Team.This role is an on-site position 4 days/week at our Sleep المزيد...

We are seeking a highly motivated Scientist to join our Research team within Regeneron Cell Medicine to support cell therapy target ID and validation and CAR-T/TCR pre-clinical research. We hope you are excited by the opportunity to help advance the next generation of cell therapies.A المزيد...

The Senior Manager Oncology Clinical Scientist leads in the development evaluation planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Senior Manager leads in a matrix environment as part of a cross-f المزيد...

The Senior Medical Director Clinical Development will play a key role in clinical development programs within the Internal Medicine portfolio focused on obesity and related comorbidities. This role serves as Scientific and Medical Lead for Clinical team(s) working closely with Operati المزيد...

Job DescriptionThe Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignmen المزيد...

As a Director in Pharmacometrics (Quantitative Pharmacology) this individual is is accountable for the delivery of support for one or more research & development programs within their pharmacometrics discipline. In this capacity the Director is accountable for the timely and accur المزيد...

TheManager Clinical Study Lead(CSL)may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design through execution to study close out. The CSL is accountable for the study المزيد...

As a Senior Manager Enterprise Architecture you will focus on supporting Standard & Architecture management and governance capabilities. This role is responsible for establishing collecting and managing a single source of truth for architecture details. In addition you will collab المزيد...

The Manager Clinical Drug Supply & Logistics is responsible for forecasting Investigational Product (IP) supply requirements for multiple clinical trials and for managing the IP distribution process to one or more clinical trials. Activities are performed on time within budget and المزيد...

The Associate Manager Clinical Drug Supply & Logistics provides support for and may be responsible for forecasting Investigational Product (IP) supply requirements for multiple clinical trials and for supporting and/or managing the IP distribution process to one or more clinical t المزيد...

This position can be on-site in Tarrytown NY or Basking Ridge NJ. This role is on-site 4 days per week and 1 day from home. A remote role is not possible for this position.The Director Resource Management (DRM) is a key liaison across multiple functions in Global Development (GD) prov المزيد...

This position is for a qualified statistician/biostatistician to support Clinical Biostatistics with Global Development.In this role a typical day might include: The incumbent will lead efforts of the Biostatistics department with cross-functional teams to articulate drug development المزيد...

The Senior Manager CDM Solid Tumor Oncology - provides oversight of lead Data Manager(s) on assigned clinical data management studies in specific therapeutic areas to assure proper planning and execution for data management deliverables that meet Regeneron standards and within timelin المزيد...

This position is for a qualified Statistician/Biostatistician to support Clinical Biostatistics within Global Development.A typical day might include:The incumbent will work with crossfunctional teams to articulate drug development questions assess the feasibility of endpoints and fra المزيد...

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

The Senior Medical Writer (SMW) works with team members and independently to write the content of clinical documents that may include CSRs protocols ICFs narratives and IBs in a variety of therapeutic areas. Opportunities to chip in to other regulatory documents may be provided. The S المزيد...

The Medical Director Clinical Development Oncology is a qualified physician scientist with exceptional academic clinical trials experience preferably in Oncology development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is r المزيد...

We are looking for a Clinical Data Manager who will serve as the DM study lead and point of contact for clinical study teams and external partners (e.g external data vendors and CROs) for multiple trials (phases 13) within a given Therapeutic Area (TA). You will oversee DM activities المزيد...