Clinical Research Coordinator - GI Division
University of California, San Francisco
Job Description TheClinicalResearchCoordinatorwilljointheGIDivisionandresponsibilitieswillincludecoordinationofclinicalresearchstudiesrelatedliverdiseaseandlivertransplantation.TheClinicalResearchCoordinatorwillperformindependentlyatthefullyoperationaljourneyleveloftheseriestoexecute,manage,andcoordinateresearchprotocols,asdirectedbythePrincipalInvestigators(PIs);maycoordinatethedatacollectionandoperationsofseveralconcurrentclinicalresearchstudiesundertheguidelinesofresearchprotocols,UCSFandregulatingagencypolicies. The incumbent will collaborate with two Principal Investigators in the GI Division—Drs. Lai and Price—on separate research studies Job Description TheClinicalResearchCoordinatorwilljointheGIDivisionandresponsibilitieswillincludecoordinationofclinicalresearchstudiesrelatedliverdiseaseandlivertransplantation.TheClinicalResearchCoordinatorwillperformindependentlyatthefullyoperationaljourneyleveloftheseriestoexecute,manage,andcoordinateresearchprotocols,asdirectedbythePrincipalInvestigators(PIs);maycoordinatethedatacollectionandoperationsofseveralconcurrentclinicalresearchstudiesundertheguidelinesofresearchprotocols,UCSFandregulatingagencypolicies. The incumbent will collaborate with two Principal Investigators in the GI Division—Drs. Lai and Price—on separate research studiesDutiesmayinclude,managementandcoordinatingthetasksofmultipleclinicalresearchstudies,actasintermediarybetweenservicesanddepartmentswhileoverseeingdataandspecimenmanagement;manageandreportonstudyresults;create,clean,update,andmanagedatabasesandcomprehensivedatasetsandreports;coordinatestaffworkschedules,assistwithtrainingofAssistantCRCs,andassistPIsupervisorwithoversightofotherresearchstaff;manageInvestigator’sprotocolsintheCommitteeonHumanResearchonlinesystem,aswellasrenewalsandmodificationsofprotocolapplicationsandtheimplementationofnewstudies;participateinthereviewandwritingofprotocolstoensureinstitutionalreviewboardapprovalwithinUniversitycompliance;helpassurecompliancewithallrelevantregulatoryagencies;overseestudydataintegrity;implementandmaintainperiodicqualitycontrolprocedures;interfacewithdepartmentstoobtainUCSFapprovalpriortostudyinitiation;maintainallregulatorydocuments;reportstudyprogresstoinvestigators;participateinanyinternalandexternalauditsorreviewsofstudyprotocols;andperformotherdutiesasassigned. Qualifications Required Qualifications: HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines Preferred Qualifications BA/BS degree in physical or biological sciences and one year of clinical research experience, or a combination of experience and education Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation Experience with electronic medical records Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.) Knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms Experience applying the following regulations and guidelines: GoodClinicalPracticeGuidelines HealthInformationandAccountabilityAct(HIPAA) TheProtectionofHumanResearchSubjects CHRregulationsforrecruitmentandconsentofresearchsubjects EffectiveCashHandlingProcedures EnvironmentalHealthandSafetyTraining FireSafetyTraining About Us About UCSF The 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. We bring together the world’s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells. Pride Values UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence – also known as our PRIDE values . In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available here . Join us to find a rewarding career contributing to improving healthcare worldwide. Equal Employment Opportunity The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. Salary Information The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement. To learn more about the benefits of working at UCSF, including total compensation, please visit: #J-18808-Ljbffr University of California, San Francisco
- University of California, San Francisco is seeking a Clinical Research Coordinator in the GI Division to coordinate liver disease studies under PI supervision. The role involves independent execution of study tasks, data collection, and regulatory compliance. Responsibilities...Geographic information system
- UCSF is seeking a Clinical Research Coordinator to join the GI Division, coordinating clinical studies on liver disease and transplantation. The role involves independent execution of study procedures, data management, and collaboration with two PIs (Lai and Price) while...Geographic information system
$34.32 - $55.19 per hour
Job Summary The Clinical Research Coordinator will independently execute, manage, and coordinate research... ...agreement rules. Benefits Information: Division of Gastroenterology Research in... ...the UCSF Division of Gastroenterology (GI). The division has a longstanding reputation...Geographic information systemHourly payFull timeWork experience placementWorldwideMonday to FridayShift workDay shift- ...Clinical Research Coordinator Responsibilities: Ensure each study patient is fully informed of the study at the time of the consent. Patient recruitment... ...Esthetics, Dietary Supplements, or Ophthalmology, or Internal Med, Infection, Obgy, Neurology, Cardiology or GI trial....Geographic information system
$161.7k - $344.4k
...Benioff Children's Hospitals Division of Pediatric Gastroenterology,... ...Nutrition Department of Pediatrics HS Clinical Faculty SeriesThe Division of... ...center and an NIH-funded GI fellowship training program,... ...Department’s mission of excellence in research, education, and patient care....Geographic information system$2,000 per month
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- ...The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to... ...the University of California, San Francisco, within the Division of Infant, Child and Adolescent Psychiatry (ICAP) at Zuckerberg...Full timeWork experience placementWorldwide
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- ...The Department of Medicine, Division of Cardiology, has developed a clinical research infrastructure within the Division. The goals are to increase industry... ...incumbent will perform duties related to the support and coordination of clinical studies and may receive training and...Full timeWork experience placementWorldwide
- ...Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the Assistant Clinical Research Coordinator will perform entry-level duties related to the support... ...of California, San Francisco and Division of Infant, Child and Adolescent Psychiatry...Full timeWork experience placementWorldwide
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$50k
...Category: Academic Staff Employment Type: Regular Job Profile: Clinical Research Coordinator II Job Summary The Department of Pediatrics is seeking a... ...more than 230 faculty members in 16 subspecialty divisions. The department promotes and enhances the health of children...Ongoing contractPermanent employmentTraineeshipWork at officeImmediate start- University of California, San Francisco seeks a Clinical Research Coordinator in the Department of Pediatrics, Division of Rheumatology, to manage and coordinate pediatric rheumatology research protocols across Oakland and San Francisco campuses. The role entails data collection...
- The Clinical Research Coordinator at UCSF's Movement Disorders and Neuromodulation division will independently coordinate multiple studies, manage data, and ensure protocol compliance under the Clinical Research Manager and PI. The CRC will support Parkinson’s disease and...
- Overview The Clinical Research Coordinator will independently or with general direction on the fully operational journey level of the series to... ...Department of Pediatrics. This role will serve within the Division of Rheumatology at both the Oakland and San Francisco campuses...Local area
$41.72 - $67.1 per hour
Senior Clinical Research Coordinator MED-VAMC-INFD Part Time 86545BR Job Summary Senior Clinical Research Coordinators independently coordinate... ...sites (Parnassus, ZSFG, SFVAHCS and Mt. Zion) and 38 divisions. Authority and accountability for the Department rests with...Hourly payFull timePart timeWork experience placementLocal areaWorldwideShift work$131.3k - $159.56k
...street operations, walking, and taxis. Division: Transit Division Section/Unit:... ..., including modeling project outcomes, research, and writing reports, applying their knowledge... ...scheduling design workshops and coordinating activities between the project and internal...Geographic information systemFull timeContract workTemporary workFor contractorsWork experience placementLocal areaImmediate startMonday to FridayFlexible hours- ...Duties include but are not limited to: coordinating with the Environmental Management Group... ...contractors and Water Supply & Treatment Division (WSTD) in-house trades for compliance... ...progress, scheduling and field meetings. Researches and reviews facility plans, historic...Geographic information systemFull timeContract workTemporary workFor contractorsWork experience placementWork at officeMonday to Friday
- ...Job Description Please note: This is a limited appointment with 18 months duration. Senior Clinical Research Coordinators independently coordinate and are accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge...Contract workLocal area
- ...integrated effort building cutting-edge hardware, software, and research capabilities to create products that can benefit millions — and... ...Serve as the main point of contact for participants in clinical trials Assist with adverse event documentation and reporting...
- ...Senior Clinical Research Coordinators with the Breast Oncology program independently coordinate and are accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge and skills. They may provide leadership to...Contract workLocal area
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$43.34 - $65 per hour
...Office-Bay Position Overview: Collects, compiles and presents clinical data for assigned area, ensuring accuracy, timeliness and accessibility of information. Maintains clinical and/or research databases for identified programs/ specialty clinics. Collects data used...Full timeWork at officeMonday to FridayShift workWeekend work- ...brain tumors). The Neuro-Oncology Service Clinical Trials Program includes pharmaceutical... ...cooperative groups, and SPORE grants for cancer research. Qualified research staff support... ...supervision of the Clinical Research Coordinator Supervisor and Research RN Manager, the...Full timeWork experience placementWork at officeLocal areaWorldwide
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