Research Scientist

Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind. We have supported many of the most impactful new drug approvals in oncology, and we are seeking the most talented individuals globally that are passionate in their desire to assist us in our mission to customize each clinical trial's imaging to optimize the opportunity to demonstrate efficacy. We are an affiliate of HonorHealth, one of the largest healthcare systems nationally, and Scottsdale Medical Imaging Limited (SMIL/RadPartners), the largest private radiology group in the United States. We are recognized as the world's largest and most preeminent iCRO in oncology.

The Nuclear Medicine Imaging Scientist is primarily responsible for conducting a variety of QC/analysis procedures and providing medical writing support at a clinical trial level. This person is responsible for reviewing the imaging data received from the clinical trial imaging sites/sponsors to confirm specific protocol requirements have been met as well as ensuring technical adequacy and data integrity. In addition, this person will assist in project management duties within the operations and medical scientific affairs departments and serve as the imaging technical support for internal and external staff. The Nuclear Medicine Imaging Scientist shall interact with external clients, internal team members, Key Opinion Leaders (KOLs), and Physician Consultant/Contracted reviewers around the development of required clinical trial documents when required. The Nuclear Medicine Imaging Scientist is responsible for assisting in the delivery of IE's central reader training, study procedures and protocol criteria when required.

Perform technical quality review of images per trial specifications

Perform Quantitative image analysis

Perform Imaging data reconstruction per trial specifications

Manage research projects and early phase clinical trials for day-day activities

Complete quality control documentation according to standard operating procedures

Develop quality control documentation in conjunction with the Project Manager

Clinical site and imaging center support

Develop training materials for imaging site personnel including Data Transmittal Form, Imaging Manual, Site Training slides, and other supplemental documents as needed

Technical training of imaging site personnel (on-site or telecon)

Develop Image QC Checklists for all studies with Nuclear Medicine as modality and assigned studies.

Collaborate with project internal teams to support sponsor specified project scope of work as required

Provide medical and scientific input to the following documents as necessary/applicable.

Project Management Plans

Image Analysis Platform

Clinical Case Report Forms

Provide training to Radiologist, Oncologist, and other sub-specialty Physicians on

Image Analysis Platform

Mentor and assist in the training of internal staff

EDUCATION AND EXPERIENCE

Registered Nuclear Medicine Technologist

Knowledge of PET/CT imaging systems required

Associates or Bachelor's degree preferred

Minimum of 3 years' experience as a nuclear medicine technologist required

Minimum of 1 year of experience in the clinical trials industry preferred

Knowledge of Good Clinical Practice (GCP), Quality Assurance/Compliance in a clinical trials setting is preferred

Image Review Charter, Imaging Manual, Data Transmittal Forms, etc.

Prior Project Management duties preferred, i.e., Service oriented approach, flexible and proactive with ability to think tactically and strategically

Self-driven, ability to develop and drive project timelines

Ability to excel in a team environment

Proficiency in MS Office and internet applications

Maintain strict confidentiality of sensitive data, records, files, conversations, etc.

Ability to motivate others and keep project teams working effectively

Ability to understand technical research protocols and successfully lead within the research environment, when required

Strong desire to be part of a dynamic, global team working closely together and growing year after year in a rewarding environment to help humanity through imaging

Commitment and caring for our fellow team members, their families, and the communities IE serves - see Caring Endpoints

we enjoy advancing clinical trials, helping patients, and celebrating success

we proof our own work, hold high standards for ourselves and our team, and always prioritize quality above all else

Travel: Up to % travel (Domestic and International)

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