Clinical Research Supervisor I

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:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe Clinical Research Supervisor I independently coordinates and is accountable for the overall administration of the Clinical Research Coordinator Core Team 3. The responsibilities include supervising and assigning duties to Clinical Research Coordinators (CRCs) and Assistant CRCs, serve on the Clinical Nuclear Imaging Research Committee (CNIRC) and coordinate and facilitate monthly meetings. The Clinical Research Supervisor I will work with Principal Investigators (PIs) to determine the level of support needed for each study and determine priorities for all team members of the CRC Core. Will monitor the studies the rest of the Core members are working on and make sure that accounts are billed on a monthly basis with the appropriate level of effort that the CRC assigned to the study dedicated for the period. u003cbr/u003eu003cbr/u003eThe Clinical Research Supervisor I will also be the subject matter expert in the area of the Institutional Review Board (IRB) submissions for the department of Radiology. Among the duties, the Clinical Research Supervisor I will evaluate research protocols, help with the IRB submission and monitor its progress as needed. u003cbr/u003eu003cbr/u003eThe Clinical Research Supervisor I will monitor the Clinical Research Billing issues for the Department of Radiology. As charges start to accumulate, the Clinical Research Supervisor I will contact the CRCs responsible for Clinical Activities in the grants to make sure that charges are properly deemed Research or Standard of Care. Additional duties will include training new CRCs and Study Coordinators that are inexperienced on IRB or other areas of research, organize CRC Core meetings, assign work to the rest of the staff and take over research duties from the rest of the staff as needed. u003cbr/u003eu003cbr/u003eIn addition to the former, the individual will independently manage multiple research studies including both industry sponsored clinical trials and investigator-initiated studies. Study management will include Committee on Human Research (CHR)/IRB submissions and maintenance, development of informed consent, creation of data collection documents, subject screening and recruitment, informed consent, subject scheduling, and collection of study data. Incumbent will work with study sponsors and facilitate investigator meetings and clinical trial monitoring visits as needed. The Clinical Research Supervisor I will provide consultation and assistance to other departments as needed regarding study start-up and study logistics. Within Radiology, will assist investigators/CRCs with OnCore/ZZ account set-up and APEX research billing review. The Clinical Research Supervisor I will train new CRCs as needed and oversee CRC Core billing and effort tracking. u003cbr/u003eu003cbr/u003eDEPARTMENT OF RADIOLOGY u0026 BIOMEDICAL IMAGINGu003cbr/u003eThe Department of Radiology is one of the largest departments in the School of Medicine (SOM) at UCSF. The mission of the Department includes research, teaching, and patient care. The Department operates across six sites in San Francisco. Major activities of the department include general Radiology, Mammography, Interventional Radiology, CT, MRI, Ultrasound and Nuclear Medicine.u003cbr/u003eu003cbr/u003eABOUT UCSF u003cbr/u003eThe University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences.,VerityZone:jobdescription,QuestionType:textarea,ActualValueFromSolar:null},{QuestionName:Organization,AnswerValue:Campus,VerityZone:location,QuestionType:select,ActualValueFromSolar:null},{QuestionName:Req Number,AnswerValue:55552BR,VerityZone:autoreq,QuestionType:text,ActualValueFromSolar:null},{QuestionName:Location,AnswerValue:China Basin,VerityZone:formtext8,QuestionType:single-select,ActualValueFromSolar:null},{QuestionName:Job Title,AnswerValue:Clinical Research Supervisor I,VerityZone:formtext10,QuestionType:text,ActualValueFromSolar:null},{QuestionName:Appointment Type,AnswerValue:Career,VerityZone:formtext12,QuestionType:radio,ActualValueFromSolar:null},{QuestionName:Percentage,AnswerValue:100%,VerityZone:formtext13,QuestionType:Text,ActualValueFromSolar:null},{QuestionName:Shift Length,AnswerValue:8 Hours ,VerityZone:formtext14,QuestionType:Radio,ActualValueFromSolar:null},{QuestionName:Shift,AnswerValue:Days,VerityZone:formtext15,QuestionType:Checkbox,ActualValueFromSolar:null},{QuestionName:Work Days,AnswerValue:Monday - Friday; 8:00 am - 5:00 pm,VerityZone:formtext16,QuestionType:Text,ActualValueFromSolar:null},{QuestionName:Required Qualifications,AnswerValue:• Bacheloru0027s degree in related area and three or more years of related experience, or an equivalent combination of education and experienceu003cbru003e• Ability to obtain certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals within one year of date of hireu003cbru003e• Broad knowledge of clinical or laboratory research and clinical research philosophy. Demonstrated ability to translate clinical research philosophy into business best practices in a trial settingu003cbru003e• In-depth knowledge of clinical research contracts and grants, clinical trials, protocols, Food u0026 Drug Administration (FDA) regulations, and complex visit structuresu003cbru003e• Project management skills to oversee the administrative operations of the clinical trials program; knowledge of strategies for recruiting human subjectsu003cbru003e• Financial analysis skills; demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgetsu003cbru003e• Demonstrated experience managing people with a wide range of educational backgrounds and skills. Demonstrated management and conflict resolution skills to effectively lead and motivate others. Demonstrated experience in training others in the field of researchu003cbru003e• Ability to perform all commonly applicable functions in word processing and spreadsheet software. Effectively uses campusu0027 clinical information and documentation application programs. Proven ability utilizing clinical trial management systemsu003cbru003e• Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently in identifying recruitment leads, implementing new strategies, and continually adjusting strategies to meet current recruitment goalsu003cbru003e• Demonstrates good problem-solving and analytical skills. Creatively addresses complex or new problemsu003cbru003e• Strong communicator; includes verbal and written, active listening, critical thinking, persuasiveness, advising and counseling skills. Clear and concise communicator. Ability to influence and negotiateu003cbru003e• Excellent interpersonal skills, including but not limited to: problem-solving, teamwork development, leadership, mentorship. Works well with others to achieve common goals. Ability to cultivate relationships with multiple stakeholders at various levels of administrationu003cbru003e• Skills to work collaboratively with other cross-functional teams. Ability to interface and collaborate with other members of an extended study team. Ability to influence/persuade. Proven ability to effectively coordinate and integrate programs with othersu003cbru003e• Ability to effectively manage multiple priorities, prioritize projects and meet the demands of a fast-paced and dynamic work environment. Adaptable to quickly changing priorities,VerityZone:formtext3,QuestionType:textarea,ActualValueFromSolar:null},{QuestionName:Preferred Qualifications,AnswerValue:• Advanced degreeu003cbru003e• Experience using database software, such as MS Access or FileMaker Pro,VerityZone:formtext4,QuestionType:textarea,ActualValueFromSolar:null},{QuestionName:License/Certification,AnswerValue:• Ability to obtain certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals within one year of date of hire,VerityZone:formtext5,QuestionType:textarea,ActualValueFromSolar:null},{QuestionName:Position Type,AnswerValue:Full Time,VerityZone:formtext6,QuestionType:radio,ActualValueFromSolar:null},{QuestionName:Department Name,AnswerValue:Radiology u0026 Biomedical Imaging,VerityZone:formtext17,QuestionType:text,ActualValueFromSolar:null},{QuestionName:Equal Employment Opportunity,AnswerValue:The University of California San Francisco is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.,VerityZone:formtext22,QuestionType:textarea,ActualValueFromSolar:null}],GQId:3093,isGQResponsive:true,isActive:true,isSocialReferralJobRestricted:false,localeId:1033,AutoOptionalReqId:55552BR,Title:Clinical Research Supervisor I,JobSiteId:5226,Link:****{Responsive_AdvancedCSS: \,Responsive_BackgroundColor: #ffffff,Responsive_BackgroundImage: ****#353a3f,Responsive_BaseFontFamily: \u0027Helvetica Neueu0027, Helvetica, Arial, sans-serif,Responsive_BaseFontSize: 16px,Responsive_ButtonBackgroundColor: #F48024,Responsive_CompiledCSS: /* remember to define focus styles! */input,select,.control,.ui-selectmenu-button,textarea,.pseudocheckbox,.pseudoradio,.controlWrapper,.textAreaWrapper,.lightBorder,.themed .ui-selectmenu-button,.ui-state-default { border-color: #353a3f;}.baseFontColor { color: #353a3f;}.baseColorPalette { background-color: #ffffff; 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