Regeneron Pharmaceuticals

The Manager Statistical Programmer will lead and support all programming activities per the project strategies within therapeutic area(s). They will work with management and study team plan and own the implementation and of programming project standard to support from the single stud More...

If youre a student pursuing a degree in Biology Chemistry Neuroscience Chemical Engineering Biomedical Engineering Mechanical Engineering or related majors you may be a fit for a Coop in our Research and Development organization.Please apply to one Coop of interest that best matches y More...

This position is responsible for establishing and maintaining procedures and policies consistent with global regulatory requirements and industry standards; and assuring training on those procedures and policies is conducted throughout the GPS department and globally. The responsibili More...

Leads the Chemistry Manufacturing and Controls (CMC) nonantibody team for cell and gene therapy technologies. The candidate will be responsible for assuring development and of global regulatory strategies for assigned cell and gene therapy portfolios. This role includes overseeing re More...

The Manager Training Operations leads development and deployment of LCoE supported Learning projects from intake tracking and reporting to closeout. We expect the Manager to use indepth learning technology and GxP training skills and knowledge to define efficient processes and solutio More...

The Associate Director Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is responsible for the effective management ofGCP GVP and GLP inspections. The GDQIM IML will engage with key stakeholders build strateg More...

At Regeneron as a working student you have many opportunities to actively contribute and gain valuable experience. Make important contacts and lay the foundation for a great career. We look forward to supporting you in developing your talent!Responsibilities:Support in the creation an 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. You will represent CP on project teams to provide strategic and scientific More...

In this role you will support HTA submissions and price negotiation primarily in Germany for specific products and their indications ensuring timely alignment on strategy with affiliate and global teams. You will provide crossfunctional input into the submission and negotiation strate More...

At Regeneron we believe that when the right idea finds the right team powerful change is possible. As we work across our growing global network to invent develop and commercialize lifetransforming medicines for people with serious diseases were establishing new ways to think about sci More...

As an Associate Director of ERP Applications Product Manager you will grow an organization designed to build the platform and systems enabling product and sustainment teams. You will be responsible for achieving the required functionality ease of and scalability across all Strategic More...

The Biostatistician implements and executes methodological and statistical aspects of clinical studies under the supervision of Therapeutic Area lead biostatistician or project lead statistician. In some cases principal function could be to develop/employ technical expertise in a part More...

At Regeneron we believe that when the right idea finds the right team powerful change is possible. As we work across our growing global network to invent develop and commercialize lifetransforming medicines for people with serious diseases were establishing new ways to think about sci More...

The successful candidate will be responsible for developing and executing regulatory strategies for biologic products including cell and gene therapy product portfolios assigned.A typical day may include the following:Responsible for CMC product development activities from a regulator More...

The GDIT Senior Manager Product Management is responsible for the implementation support and enhancement of GD technology products for Development Operations & Portfolio Management (DO&PM) focusing on Clinical Operations Shared Services and Study Startup. You will collaborate 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...

The Global Patient Safety (GPS) Lead role (Director of GPS) serves as the first point of contact (POC) for all safety related issues for the compound(s) asset(s) assigned within a given therapeutic area (TA) and is the GPS representative on the cross functional strategic program team 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 Internal Medicines Therapeutic Area (TA). You will be responsib More...

This role resides in the Global Development area of Regulatory Affairs Global Patient Safety and Development Quality RA GPS and DQ) and the Director of Strategy Planning and Operations role will work closely with the Senior Director and the broader Strategy Planning & Operations t More...

The Vice President (VP) of GPS Operations is responsible for overseeing the global pharmacovigilance areas of Case Evaluation and Reporting (CER) Quality and Compliance Center of Excellence (CoE) ensuring the effective operations and compliance across our portfolio lifecycle and geogr More...