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Clinical Research Coordinator C (Radiology)
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Posted Job Title
Clinical Research Coordinator C (Radiology)
Job Profile Title
Clinical Research Coordinator C
Job Description Summary
This position will be responsible for supporting research within Nuclear medicine and Molecular Imaging division of the department of Radiology including the initial set-up and technical review to develop imaging protocols and documents related to implementation of the nuclear medicine procedures. Responsibilities may include regulatory filings, CRF development, carrying out study visits, database development and data entry, implementation of imaging protocols and carrying out nuclear medicine procedures. Responsibilities will include operationalizing study protocols and procedures, correspondence with sponsors and/or investigators regarding start up and study management, communication with internal UPenn regulatory bodies and external regulatory agencies (e.g. FDA, sponsor or CROs). This position will also include tasks that require a nuclear medicine technologist certification (active certification must be maintained) to set up and run imaging protocols on scanners that may include PET/CT and SPECT/CT, place IVs, prepare radiopharmaceutical doses for injection and perform radiopharmaceutical injections, as appropriate, with or without the supervision of a nuclear medicine authorized user. Other technical tasks may include camera QC procedures, phantom imaging, reconstructing image data, uploading images to external web portals, completion of scanner qualification phantoms or other test scans. Tasks will include working closely with PET Center Administrative director, Principle Investigators and other staff in the unit and in collaborating departments and staff within the nuclear medicine clinic to plan and implement study procedures, collect and monitor data and report study progress internally and to study sponsor. Responsible for preparation and submission of IRB and other regulatory submissions, correspondence and organization and maintenance of regulatory documentation following good clinical practice guidelines for conduct of research involving human subjects. This position will oversee or perform data entry, aid in resolving data queries, schedule and carry out study visits.
Job Description
This position will be responsible for supporting research within Nuclear medicine and Molecular Imaging division of the department of Radiology including the initial set-up and technical review to develop imaging protocols and documents related to implementation of the nuclear medicine procedures. Responsibilities may include regulatory filings, CRF development, carrying out study visits, database development and data entry, implementation of imaging protocols and carrying out nuclear medicine procedures. Responsibilities will include operationalizing study protocols and procedures, correspondence with sponsors and/or investigators regarding start up and study management, communication with internal UPenn regulatory bodies and external regulatory agencies (e.g. FDA, sponsor or CROs). This position will also include tasks that require a nuclear medicine technologist certification (active certification must be maintained) to set up and run imaging protocols on scanners that may include PET/CT and SPECT/CT, place IVs, prepare radiopharmaceutical doses for injection and perform radiopharmaceutical injections, as appropriate, with or without the supervision of a nuclear medicine authorized user. Other technical tasks may include camera QC procedures, phantom imaging, reconstructing image data, uploading images to external web portals, completion of scanner qualification phantoms or other test scans. Tasks will include working closely with PET Center Administrative director, Principle Investigators and other staff in the unit and in collaborating departments and staff within the nuclear medicine clinic to plan and implement study procedures, collect and monitor data and report study progress internally and to study sponsor. Responsible for preparation and submission of IRB and other regulatory submissions, correspondence and organization and maintenance of regulatory documentation following good clinical practice guidelines for conduct of research involving human subjects. This position will oversee or perform data entry, aid in resolving data queries, schedule and carry out study visits.
Position contingent upon funding.
Qualifications
Bachelor's Degree with 4-6 years of related experience in research and clinical study methodologies or equivalent combination of education and experience is required
Working Conditions
Office, Library, Computer Room; Requires extensive safety
Physical Effort
Typically sitting at a desk or table; Occasional lifting 25 lb. or less
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$50,684.00 - $91,232.00
Affirmative Action Statement
Penn adheres to a policy that prohibits discrimination on the basis of race, color, sex, sexual orientation, gender identity, religion, creed, national or ethnic origin, citizenship status, age, disability, veteran status, or any other legally protected class.
Special Requirements
Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
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