SUMMARYImaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the CureTM. Everything we do is aligned with this singular purpose. 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.Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; North Harrow, UK; Leiden, Netherlands; Basel, Switzerland; Hyderabad, India and Shanghai, China. 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 Medical Director, Imaging is primarily responsible for managing the development of essential documents and processes related to image analysis, reader training and reader performance for clinical trials in accordance with IE’s requirements.RESPONSIBILITIESOversees, performs and/or assists with medical/scientific project deliverables for imaging studies in clinical trials in accordance with the project scope of work and within sponsor required timelines including but not limited to:Review Protocols, Imaging Review Charters, Imaging Manuals, Image QC Guidelines, Reader Rules and Read QC GuidelinesReview trial configuration specifications as it relates to image analysis platforms for specific analysis criteriaReview training materials, training modules, and perform training for internal IE staff, blinded independent central review (BICR) readers, and site radiologistsRadiology and Medical review of BICR data to ensure central reader competence and adherence to study requirementsReview development of reader performance metrics plans and review performance dataDesign, review, and approval of study-related interim or final reportsProvides support to internal IE staff on the QC of images and BICR reads based on expert radiological and criteria skillDevelop expertise, maintain knowledge and train others in the use of IE’s image analysis platforms as it relates to the performance of BICR readsProvide education and training to staff for development of key study documents, processes, and response criteriaCollaborate with internal project teams to support sponsor specified project scope of workAssist with projects related to IE’s research and technology development studies as requestedPerform other duties as assignedEDUCATION AND EXPERIENCEMD/ radiology degree required, PhD in medical or health science preferredMinimum of 7 years of experience in clinical research and medical imagingMinimum of 5 years of experience working with the pharmaceutical industryMinimum of 5 years within an imaging core lab (an imaging CRO) with oncology experienceSKILLSExpert knowledge of radiologic imaging modalities and assessments related to efficacy endpoints common to clinical trials with emphasis in oncologyExpert knowledge of FDA Guidance documents related to imaging and knowledge of the regulated environment apicable to an imaging core lab and the pharmaceutical drug development industryAbility to understand technical research protocolsWork precisely according to all procedures, rules, and regulationsMust have superior attention to detail and excellent oral and written communication skillsCoaching, mentoring, and developmentAbility to think strategically and tactically and develop ans accordinglyHands-on service-oriented approach, flexible and proactive towards adapting to clients’ needsAbility to manage project activities with diverse groups and individualsAbility to excel in a team environmentMust have the ability to multitask and work under pressureMust have strong time management and organizational skills. Prioritizing workload according to the changing needs of the day to day business is criticalMust maintain strict confidentiality of sensitive data, records, files, conversations, etc.Self-motivated and able to grasp new concepts quicklyProficiency in MS office and internet applicationsIMAGING ENDPOINTS’ TEAM CHARACTERISTICSPassion to Connect Imaging to the CureTM and pursue a meaningful career by improving the lives of cancer patients through imagingStrong 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 imagingCommitment and caring for our fellow team members, their families, and the communities IE serves – see more information about Caring Endpoints at Website and high ethical standards; we always do the right thingHigh intellect and ingenuity; we enjoy solving problems, finding a better way, and the challenge of making a difference by improving livesStructured, organized, detail-oriented, and self-motivated; we approach each day with a detailed plan and excitement to accomplish the day’s objectives while striving to improve ourselves and IEAccountable; we do what we say and communicative effectively to meet deadlines; we enjoy advancing clinical trials, helping patients, and celebrating successHigh standard for excellence; we proof our own work, hold high standards for ourselves and our team, and always prioritize quality above all elsePHYSICAL REQUIREMENTSWhile performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms and talk and hear. The employee is frequently required to sit. Specific vision abilities required by this job include close vision, color vision, ability to adjust focus.Travel: 10-20% travel (Domestic and International) #J-18808-Ljbffr