Associate Director, Clinical Imaging (Oncology)
- Location
- TARRYTOWN; Remote - United States; Boston; Warren
- Work mode
- Remote
- Employment type
- Full-time
About the job
Build Our Future Together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. As An Associate Director, Clinical Imaging you will lead the strategy and execution of complex early and late phase oncology imaging in clinical trials where imaging plays a key role. Imaging includes all modalities with a special focus on PET and CT. In this role, you will champion the development of imaging endpoints/biomarkers and drive the scientific imaging aspects as well as tumor response assessment of oncol ogy clinical studies.
The successful candidate will be an independent imaging scientific leader and a member of cross-functional program teams including Regeneron clinical and preclinical colleagues as well as external academic and industry partners. This position provides excellent opportunities to develop innovative imaging endpoints and biomarkers in support of clinical development and bringing new treatment options to patients.
When & Where Our preference for this position would be to have someone on-site in our Tarrytown, NY offices 4 days per week. However, we are also open to a remote hire for an exceptional candidate.
Discover Your Role
- Create fit-for-purpose imaging biomarker strategies and work closely with research, clinical imaging and the oncology therapeutic area for the development of imaging endpoints to inform and advance the Regeneron clinical pipeline.
- Prepare and present clinical imaging strategies to senior management.
- Manage a complex network of stakeholders across Regeneron.
- Lead, design and implement multi-modality imaging measures as endpoints for oncology therapeutic clinical studies.
- Collaborate closely with Regeneron clinical teams as imaging subject matter expert to ensure optimal design and execution of imaging strategy including development of protocols, imaging manuals and charters, statistical analysis plans and clinical study reports.
- Work closely with Clinical Imaging Operations and imaging contract research organizations to ensure the flawless conduct and data integrity of studies’ imaging components and endpoints.
- Serve as Study Imaging Director on clinical trials focused on qualification and utilization of novel imaging biomarkers.
- Design and implement novel PET, immuno-PET and other novel imaging agents/biomarkers in oncology clinical trials.
- Lead the interaction with regulatory agencies for communications regarding imaging endpoints and procedures.
- Lead the interaction with regulatory agencies and site ethics committees for approval of clinical imaging biomarker development studies.
This Role Requires
• PhD with a minimum of 7+ years of clinical imaging experience (minimum of 5 years within oncology drug development).
- PhD with a minimum of 7+ years of clinical imaging experience (minimum of 5 years within oncology drug development).
- Experience implementing central efficacy assessments using tumor response criteria such as RECIST 1.1, iRECIST, PCWG3, Lugano and IMWG in oncology clinical trials is required.
- Successful engagement experience with regulatory agencies and the ability to champion imaging innovations and lead projects effectively.
- 7+ years of imaging experience in oncology drug development and clinical PET tracer development in a pharmaceutical/biotechnology setting preferred.
- Experience as study scientific director of PET imaging biomarker clinical trials in Oncology preferred.
- Experience with radiopharmaceuticals and applying imaging as a quantitative endpoint in clinical and preclinical studies in Oncology preferred.
- Imaging CRO oversight and implementation of quality control procedures preferred.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually) $176,100.00 - $287,300.00
From Regeneron Pharmaceuticals's careers page (Workday), checked 5 Nov 2026.
How to apply
- Select Apply on regeneron.com. It opens Regeneron Pharmaceuticals's own application form in a new tab, run on Workday.
- Fill in the form and upload your résumé there. Jobiwork never sees your application.
- Regeneron Pharmaceuticals will reply to you directly. No real employer asks you for money to apply.
Posted 5 Nov 2026 · checked 5 Nov 2026 · Report this job