Regeneron Pharmaceuticals Inc.
Director, Precision Medicine, Companion Diagnostics
Regeneron Pharmaceuticals Inc., Basking Ridge, New Jersey, us, 07920
We are seeking a Director to join our Precision Medicine team. The Director, Precision Medicine will lead Companion Diagnostics (CDx) strategy working closely with the Senior Director, Precision Medicine CDx and key cross-functional collaborators to deliver innovative diagnostics solutions in support of Regeneron programs. The primary role will be to guide strategy for patient selection/stratification, passionate about immunohistochemistry (IHC), and lead implementation and execution of CDx assays (from study conduct, sample management testing to launch) in collaboration with partners/IVD Sponsors and central testing laboratories to support early and late-stage programs within our oncology pipeline.
As a Director, a typical day may include the following: Define innovative diagnostic strategies and propose projects from idea to implementation taking into consideration all relevant inputs. Develop strong relationships and partnerships with IVD partners and testing laboratories. Oversee operational aspects of CDx clinical trial implementation, manage timelines, and communicate effectively both externally and internally. Have relevant knowledge of regulatory requirements (including IVDR) and support regulatory teams surrounding CDx (from study set up to PMA filing). Have a solid understanding of Performance Study requirements and make strategic decisions and drive delivery in coordination with IVD regulatory counterparts. Be viewed as a subject matter expert in oncology and effectively communicate with clinical study teams on program direction. Able to define and drive CDx strategy and effectively gain alignment across relevant partners (including senior management) within Regeneron. Lead execution and implementation of Regeneron CDx strategy in collaboration with key partners. Evaluate and make decisions on technologies and vendors as needed to support diagnostic and program deliverables. Provide testing site implementation and oversight for CDx programs from contracting to sample logistics to data delivery.
This role may be for you if: You possess strong leadership tendencies, ability to proactively identify problems, determine resolutions, set priorities, and direct projects and work cross-functionally to manage expectations with excellent communication and collaborative skills and work well in a team-based environment. You demonstrate strong leadership skills and possess a high level of emotional intelligence and effectively work collaboratively with colleagues, vendors, and internally at Regeneron to ensure program success. Lead team members in representing Regeneron and working with colleagues from allied companies to develop and implement Precision Medicine CDx strategies.
To be considered for this role, you must have a Ph.D. and/or M.D., with a minimum of 10 years postdoctoral experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams. Extensive experience in diagnostic development with demonstrated success in a drug development setting is required. We need a strong understanding of technical, regulatory, clinical, and strategic aspects of diagnostic delivery. We are seeking CDx knowledge, demonstrated deep knowledge in science and technology, and demonstrated experience in delivering diagnostics. Contributes to and reviews documents pertaining to regulatory interactions and filings related to Precision Medicine, including product labeling and participates as appropriate in internal and external meetings.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually) $198,000.00 - $330,000.00
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As a Director, a typical day may include the following: Define innovative diagnostic strategies and propose projects from idea to implementation taking into consideration all relevant inputs. Develop strong relationships and partnerships with IVD partners and testing laboratories. Oversee operational aspects of CDx clinical trial implementation, manage timelines, and communicate effectively both externally and internally. Have relevant knowledge of regulatory requirements (including IVDR) and support regulatory teams surrounding CDx (from study set up to PMA filing). Have a solid understanding of Performance Study requirements and make strategic decisions and drive delivery in coordination with IVD regulatory counterparts. Be viewed as a subject matter expert in oncology and effectively communicate with clinical study teams on program direction. Able to define and drive CDx strategy and effectively gain alignment across relevant partners (including senior management) within Regeneron. Lead execution and implementation of Regeneron CDx strategy in collaboration with key partners. Evaluate and make decisions on technologies and vendors as needed to support diagnostic and program deliverables. Provide testing site implementation and oversight for CDx programs from contracting to sample logistics to data delivery.
This role may be for you if: You possess strong leadership tendencies, ability to proactively identify problems, determine resolutions, set priorities, and direct projects and work cross-functionally to manage expectations with excellent communication and collaborative skills and work well in a team-based environment. You demonstrate strong leadership skills and possess a high level of emotional intelligence and effectively work collaboratively with colleagues, vendors, and internally at Regeneron to ensure program success. Lead team members in representing Regeneron and working with colleagues from allied companies to develop and implement Precision Medicine CDx strategies.
To be considered for this role, you must have a Ph.D. and/or M.D., with a minimum of 10 years postdoctoral experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams. Extensive experience in diagnostic development with demonstrated success in a drug development setting is required. We need a strong understanding of technical, regulatory, clinical, and strategic aspects of diagnostic delivery. We are seeking CDx knowledge, demonstrated deep knowledge in science and technology, and demonstrated experience in delivering diagnostics. Contributes to and reviews documents pertaining to regulatory interactions and filings related to Precision Medicine, including product labeling and participates as appropriate in internal and external meetings.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually) $198,000.00 - $330,000.00
#J-18808-Ljbffr