Regeneron Pharmaceuticals

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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...

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...

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...

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...