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Scientist I, Radiopharmacology

Champions Oncology, Inc.
Full-time
On-site
Rockville, MD
$80,000 - $96,000 USD yearly
Clinical Research and Development

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Role Summary

Scientist I, Radiopharmacology

Responsibilities

  • Design and execute radiolabeling reactions using a range of isotopes, including Lu-177, Ac-225, In-111, Zr-89, At-211, I-131, and Pb-212.
  • Perform conjugation reactions between bifunctional chelators and peptides or proteins.
  • Develop and optimize radiochemical synthesis protocols for both diagnostic and therapeutic applications.
  • Conduct quality control and stability testing of radiolabeled
  • Analyze experimental data, interpret results, and communicate findings to cross-functional teams.
  • Support preclinical research studies, including biodistribution, pharmacokinetics, and dosimetry assessments.
  • Prepare, review, and ensure compliance of study protocols and technical reports
  • Train and mentor junior staff in radiochemistry techniques, radiation safety, and handling of radioactive materials.
  • Maintain accurate laboratory records
  • Stay current with advancements in radiochemistry, nuclear medicine, and isotope production technologies.
  • Assist in the evaluation and implementation of new equipment, automation systems, and analytical tools.
  • Other duties may be assigned verbally at any time.

Qualifications

  • PhD in a relevant field (e.g., radiochemistry, chemistry, biochemistry, pharmaceutical sciences).
  • Expertise in radiochemistry, radiobiology, molecular imaging, and therapeutic radionuclide production.
  • Experience with analysis and interpretation in vivo data of radioconjugates.
  • Strong computer, organizational, and multitasking skills.
  • Excellent communication skills.

Skills

  • Expertise in radiochemistry, radiobiology, molecular imaging, and therapeutic radionuclide production and handling.
  • Expertise in chromatography techniques such as thin-layer chromatography (TLC), column chromatography, high-performance liquid chromatography (HPLC).
  • Expertise in conducting in vivo studies using radiolabeled compounds
  • Experience with analysis and interpretation in vivo data of radioconjugate pharmaceuticals.

Education

  • PhD in a relevant field (e.g., radiochemistry, chemistry, biochemistry, pharmaceutical sciences).
  • Expertise in radiochemistry, radiobiology, molecular imaging, and therapeutic radionuclide production.
  • Experience with analysis and interpretation in vivo data of radioconjugates.
  • Strong computer, organizational, and multitasking skills.
  • Excellent communication skills.

Additional Requirements

  • Must be able to sit and use hands to finger, handle and feel.
  • Must be able to lift and move packages weighing up to 50 pounds.
  • Must be able to sit for long periods of time using a computer in a typical office environment in a multi-level facility.
  • Some activities require repetitive motion and reaching, pulling, or pushing.
  • In carrying out the duties of the job there will be frequent exposure to fumes and chemical hazards
  • Duties performed routinely require exposure to blood, body fluid and tissue.
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