70 jobs found in Tarrytown

The Manager, Talent Acquisition is integral to Regeneron's continued successful expansion and an important contributor as part of our Global Recruiting Team. You will partner directly with our Global Development and Clinical Operations business units on talent strategies that deliver outstanding candidates and experiences across the entire span of a full-cycle recruitment program. This is an opportunity to work with one of the fastest growing, most innovative organizations in the Biotech / Pharma industry and you'll have an immediate and direct impact on Regeneron's most important resource...our employees. As a Manager, Talent Acquisition a typical day might include the following: Working collaboratively to source, identify, qualify and deliver candidates for the assigned client groups; including senior-level positions, using a variety of creative recruiting methods. Partnering with Hiring Managers and HR Business Partners to identify and clarify job specifications in order to...

The Senior Manager Sourcing - Supplier Risk and Diversity will develop, implement and oversee Regeneron's global risk management and supplier diversity activities related to the enterprise supplier management program. We are looking for someone to be responsible for risk analysis of critical suppliers to ensure continuity of supply. While working with Regeneron partners, you will manage relationships to promote supplier risk and diversity awareness and ensure accurate execution and compliance with standards, policies and procedures. We need a manager who is comfortable reporting and presenting to senior management. A typical day may include: • Communicate to business units and cross-functional teams' significant third-party events and call out to senior management as needed. • Lead and/or work with others to seek issues where analysis requires an understanding of current business trends and industry benchmarks. • Use sophisticated analytical tools, discernment, thought leadership...

This Senior HRBP role will support the Global Development Operations and Portfolio Management function and is a senior member of the Sciences HR Business Partner team. The Global Development organization is located primarily in Tarrytown and Basking Ridge, NJ, with a growing ex-US footprint in the UK and Ireland. Key focus is on becoming an advisor to executives, managers and employees on organizational and people related issues. This may include: workforce planning, DE&I, change management efforts, organization design and efficiency, employee engagement, employee relations, and performance management to promote and maintain REGN's high-performance culture...what we call the Regeneron Way. Deep knowledge of the biopharmaceutical business and ability to interact with physicians and scientists (and physician scientists!) and use of data is a must in this role. You will be a sounding board for the business, evaluating and influencing the effect of business decisions on people, and...

Our Medical Account Specialists are at the forefront of engaging Medical Oncologists and other key customers. We need someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right - aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented team if you are up for the challenge. As a Medical Account Specialist, a typical day may include: Develop strategy and execute tactics within key designated accounts in the Oncology therapeutic area to establish, generate and expand market share Responsible for crafting and maintaining Account Profiles. (Hospitals, Clinics, Infusion Centers, KOL's, Target HCPs, HCPs, etc.) Proactively identifies business opportunities with and leads appropriate coordination of effort...

The Medical Director crafts clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials. He/she is accountable for results of clinical trials under her/his direct responsibility. .She/he also contributes to the Clinical Development Plan (CDP) that meets international regulatory standards, conducts literature and database research on trials as needed. He/she works in collaboration with Clinical Project Managers and Clinical Trial Managers at the study level, and with Therapeutic Area Program Managers. She/he contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings. A typical day may involve the following: Defines clinical trial-related goals and objectives. Ensures the relevance and accuracy of medical science underpinning of clinical study concepts (CSCs) based on thorough review and consultation with specialists. Reviews,...

The Manager Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases. We will expect this to include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment. A typical day might include the following: Complete signal detection activities in line with approved safety surveillance plan Perform signal evaluation for any identified signals and author the safety evaluation reports Manage preparation and review of safety documents including DSUR, PSUR, RMP, response to health authority or other queries Prepare and deliver presentations at SMT meetings; participate in clinical study team meetings for assigned molecules Participate in other risk management activities as appropriate for assigned compounds We may ask you to represent GPS on cross-functional teams, including Regeneron Safety Oversight Committee, Independent Data...

We are seeking an experienced, motivated research associate to join our team of scientists in the Velocigene department. Using cutting edge methods to generate genetically modified mouse and rat ES cells, and human iPS cells, the Velocigene technology platform gives Regeneron unprecedented speed and capacity for the validation of therapeutic targets and the creation of new genetically engineered models of human disease. The Research Associate will be a key member of the ES cell engineering pipeline. In this role, a typical day may include: • Optimize and implement robotic automation solutions into the ES cell engineering pipeline. • Propose and develop new methods or technology innovations that improve our discovery capabilities. • Interact on a regular basis with lab members and higher-level Scientists to accomplish research goals. • Contribute to lab upkeep to help maintain an effective and efficient working environment. • Communicate experimental results and conclusions to...

We are looking for a motivated individual to join the Research Management & Operations group to assist in the operational support of R&pD for key areas involving Facilities, Procurement, IT, Legal and enterprise initiatives. This person will have close interaction with end users and stakeholders to keep our scientific efforts moving forward with efficiency while addressing challenges as they arise. In this role, a typical day may include: • Work closely with Facilities Asset Management, R&D Finance, and Procurement to manage proper oversight of contracts including timely execution, accurate invoicing, and communication to relevant R&pD stakeholders • Assist with efforts to supervise lab equipment utilization and recommend efficiency opportunities and space management solutions through use of cores and other asset sharing • Alongside Facilities and Automation Core identify opportunities for freezer storage and other sample management • Regularly set up...

We are actively looking for a Senior Financial Analyst to join our rapidly growing team. This individual will be an integral member of the FP&A team, supporting the G&A Finance organization at Regeneron. This person will support the Finance Leads for several G&A functions, most notably the Human Resources and Law Departments. The SFA will be a strategic member of the G&A Finance team and will primarily be responsible for preparing annual budgets and quarterly forecasts. In addition, this person will act as a cost center controller and analyze actual to budget variances, prepare monthly reporting packages, and assist the Finance Leads with ad-hoc reporting and analysis as needed. The SFA will assist the G&A Finance team with forecast and budget data inputs as well as being tasked to identify and implement improvements with current departmental procedures. A typical day might include the following: Partnering with the G&A Finance team to prepare annual...

The Director, Patent Attorney will act as Legal Counsel on matters related to the development, protection, and management of Regeneron's valuable intellectual property pertaining to its manufacturing. The role will be responsible for patent activities relating to manufacturing and bioprocessing at all stages of the development pipeline including cell line technologies, purification, formulations, assay and media development. This position will partner closely with our world-class scientists and manufacturing development leaders around key strategies for our rapidly growing patent portfolio, patent filings, trade secret protection, and patent actions. As a Director Patent Attorney, a typical day may include: Identifying, capturing and prosecuting new inventions relating to manufacturing and bioprocessing; Preparing and prosecuting global patent applications relating to all aspects of manufacturing & bioprocessing including cell development, cell culture, purification, assay...

The Associate Web Specialist is responsible for supporting and contributing to various web-based applications used for the administration of independent medical education funds awarded by Regeneron. This position will also provide reporting services including data intensive deliverables and audit readiness functions. You will serve a resource for and collaborate with internal and external partners. A typical day may include: Working with the Medical Education team to identify, define, and verify issues with current systems Collaborateing with internal partners and external vendors to troubleshoot solutions Producing queries to ascertain accurate formatted data as requested within multiple systems Compliantly collaborating with internal partners, grant recipients, and external vendors for user training and issue troubleshooting Collaborating with graphic services to improve the user experience of various web-based applications Actively participate in and contribute to...

We are looking for an Animal Research Associate to join the VelociGene team. This person would manipulate, observe and care for genetically altered rodents to prepare them for study. In this role, a typical day may include: • Performs certain basic tasks vital for the processing of genetically altered rodents such as animal identification by marking, breeding, weaning, and collection of tissue samples for DNA or RNA analysis. • Performs a natural history analysis when requested. • Records crucial data in the Velocigene Data Management System. • Handles other responsibilities including, but not limited to, the breeding of rodents serving as embryo donors and recipients. • Performs husbandry (cage changing) duties. • Performs additional responsibilities related to the packing and shipping of rodents as well as some basic vivarium tasks such as ordering supplies, and general maintenance when needed. This role may be for you if you: • Are looking to further their skills and...

The Immunization team within the Therapeutic Antibody group is looking for an R&D Specialist who will work with VelocImmune® mice for the development of therapeutic monoclonal antibodies and antibody reagents to support research and pre-clinical programs. This position involves about 50-60% in-vivo work. In this role, a typical day might include performing the following: Execute immunization experiments according to established protocols. Conduct immuno-assays to determine immune responses, analyze the data and communicate the results with upper managers. Collaborate with antibody isolation teams to conduct the final boost in a timely manner. This job might be for you if: You enjoy working productively in a fast-paced collaborative environment. You have an eye for detail and pride yourself on the quality of your work. With your sleeves rolled up, you work on current problems while thinking of future solutions. You have strong communication skills. To be...

This position will report to Director of Transfer Pricing and will support Regeneron's overall tax initiatives through preparation of transfer pricing and planning analyses, including documentation for compliance and planning purposes. The candidate will possess strong interpersonal skills and the ability to collaborate within the Tax department as well as across functions, sites and other teams within Regeneron's business. Skills that will make a candidate successful in this role will be strong quantitative, organizational, and written and verbal communication skills. As an Associate Manager, Transfer Pricing a typical day may include: Analyzing, modeling and assisting with the implementation of tax strategies (e.g., licensing, cost share, profit splits); Conduct quarterly and annual profitability reviews of results; Support for transfer pricing components of tax returns as needed. Develop transactional facts and facilitate the documentation process for Regeneron's...

The position with the Regulatory and Commercial Law team will provide proactive and collaborative legal support in connection one or more of Regeneron's products and will act as a legal advisor to our commercial operations, sales, marketing, medical affairs, regulatory, and compliance teams. The role will counsel our internal partners through a deep understanding of healthcare laws, including the Food, Drug and Cosmetic Act, and laws related to the discovery, development, sales and marketing of biotechnology products (including healthcare fraud and abuse laws). The ideal candidate will have relevant in-house experience counseling on an approved product and providing practical and strategic legal advice on a broad range of issues. As an Associate Director/Director, Corporate Counsel, a typical day may include: Providing product support counseling for one or more of Regeneron's products/product candidates from development through commercialization and lifecycle planning Counseling...

The Sr. Manager, Pricing and Contracting Analytics will play a critical role in supporting the day to day operations of the Pricing group and providing broad analytical support to evaluate payer and provider contracting strategies. This role will work closely with the Brand Pricing Strategy leads to support all pricing and analytics requirements. Responsibilities: Provide analytics support for establishing Payer and Provider Strategies for assigned brands Perform Payer Account specific pre and post deal analytics, synthesize insights and help develop power point slides; analysis will incorporate implications to GTN, ASP etc. Develop year-over-year trends and benchmarks using payer analytics reports, and conduct and create product utilization analysis and reports by customer segments, to build ROI models and competitive insights Build ASP and managed care forecast models to support brand and LCM pricing and contracting strategies Engage with sales forecasting and analysis,...

The Director Regulatory Affairs - Oncology will provide leadership on global clinical regulatory activities. Responsibility will mainly focus on regulatory filings and on providing strategic as well as operational leadership for the project teams in oncology. In addition, responsibilities will include support to ongoing clinical activities. The candidate will contribute and/or lead IND/CTA and BLA submissions activities for Regeneron's clinical oncology candidates. In this role, a typical day might include the following: This role requires the ability to integrate and apply knowledge of global regulations governing pharmaceutical drug development of all aspects of Regeneron's quality, preclinical and clinical drug development programs, policies and procedures, so that Development teams can meet all objectives within specified timelines and so that the state of compliance is maintained to all regulatory commitments/requirements. Develop regulatory strategies for assigned...

We are looking for an independent Sr Administrator Coordinator to provide support to the SVP, VP, Senior Leadership Team as well as Global Strategic Sourcing & Procurement. This role will require knowledge of company practices and procedures, problem-solving and candidates must consistently exercise considerable judgment and initiative. In this role a typical day may include: • Proactively manages calendars using detailed understanding of department and leadership priorities. • Fully responsible for execution of internal and external meetings. Responsible for collaborating with Strategic Sourcing and Procurement to manage contracts for off-site meetings as well as managing meeting/event budgets within the approval limit. • Anticipate and make recommendations for catering for meetings and events scheduled over meal periods. Where applicable, assist employees and guests with travel and expense reports. • Advanced knowledge of company policies, procedures and resources and...

The Associate Manager of Regulatory Intelligence supports and coordinates Regulatory Intelligence (Reg Intel) proactive global monitoring and surveillance activities of the full drug development lifecycle from preclinical through commercialization. This position may have limited exposure in supporting initial draft comments on key regulatory documents and requirements (e.g. regulations, guidance, directives, etc) to global Health Authorities. In this role, a typical day will have the following responsibilities: We are seeking an Associate Manager of Reg Intel who can lead the collection, build at, maintain and distribute regulatory newsletter content to the organization. He/She also owns the content of and updates to the Regulatory Intelligence SharePoint and RON sites (e.g. tracking industry meetings and events). In addition, we need this role to support internal partners with the collection and distribution of requested regulatory intelligence queries or information on less...