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4 jobs found in Hicksville, NY

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Research Hicksville, NY
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Dana-Farber Cancer Institute  (1) U.S. Renal Care  (1) Montefiore Medical Center  (1) Glens Falls Hospital  (1)
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GF
Sep 14, 2026
Medical Physicist - Radiation Oncology
Glens Falls Hospital New York, NY
Job Description Compensation : $84.13 - $116.34 per hour (Calculated from the $175,000 - $242,000 base range). Exact rate is determined on a case-by-case basis commensurate with experience level, as well as education and certifications pertaining to each position which may be above the listed job requirements. The Impact You Can Make The medical physicist works independently to provide medical physics support for the Radiation Oncology Department. In addition, provides medical physics support to Medical Imaging and other departments that utilize radiation producing equipment or radioactive material. How You Will Fulfill Your Potential ( Responsibilities) Perform Intensity Modulated Radiotherapy (IMRT) & conventional 3D treatment planning. Review weekly patient charts & participate in chart rounds. Perform in-vivo dosimetry. Perform patient specific IMRT QA, second check of IMRT, and conventional treatment plans. Execute manual calculation checks on...
Laboratory Medical Imaging Research
MM
Aug 20, 2026
Academic/Faculty/Research Physician
Montefiore Medical Center New York, NY
Allergist - Clinician-Educator Track Children s Hospital at Montefiore/Albert Einstein College of Medicine Bronx, New York The Division of Allergy and Immunology in the Department of Pediatrics at The Children s Hospital at Montefiore (CHAM) and the Albert Einstein College of Medicine (Einstein) is seeking candidates to join our dynamic and growing faculty. CHAM is a quaternary care, academic children s hospital in New York City, serving the diverse patient population of the Bronx, Westchester County, and the Hudson Valley. Our division is seeking an American Board of Allergy and Immunology (ABAI) Certified or Eligible Allergist/Immunologist to join our faculty. The Division currently includes five full time physicians, four fellows, one nurse practitioner, three nurses, and other support staff to service a very active clinical program with over 6,000 outpatient visits per year at three office settings. We manage the spectrum of allergic and immunologic diseases including but not...
Physician & Surgeon Research
Dana-Farber Cancer Institute
Jul 16, 2026
Full Time
Senior Clinical Research Coordinator - Milford
Dana-Farber Cancer Institute Milford, CT
The Senior Clinical Research Coordinator (CRC) will work within the Dana-Farber Milford Satellite location and support the clinical research program and research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The Senior CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and...
Research
US
Sep 12, 2026
Full Time
Clinical Research Coordinator
U.S. Renal Care Orange, CT
Responsibilities: SUMMARY The Clinical Research Coordinator (CRC) is responsible for the coordination of daily clinical trial activities. USRC has a research Partnership with the principal investigator (PI) and their physician practice. The local oversight and direction for activities related to the conduct of the clinical research is directed by the PI. The CRC will work collaboratively with the principal investigator (PI), the Sr. Clinical Research Coordinator (SCRC), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations. The CRC will assist the PI in protecting the rights, safety and welfare of all study participants....
Research
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