This is a contract job opportunity. potential for perm.
Position: Clinical Trial Assistant 8924
Location: Madison WI
Schedule: M-F 8 am - 5 pm
Projected duration: 6 months + potential for perm
Job code: CVDJP00028924
Benefits are available
pay rate - $21 to $23 per hour depending on experience
Essential job duties:
¨(20%) Data Planning – responsible for all data aspects of studies including review of draft protocols,attendingClinicStartUpMeetings,supportingthe workbook(CRF) designprocess, training plans for non-standard study data capture and attend Biometrics start up meetings as required.
¨(20%)EnsurethatthedataentryandQC ofdoseescalationdataiscompletedwithinthe required timelines.
¨(15%)CompletedailyongoingQCofallstudydataacrossClinicalOperations includingdaily shop floor QC.
¨(15%)ActasprinciplehostforsponsorCRFmonitoringvisits.Promotingaprofessionalimage of Leeds CRU and building strong collaborative working relationships with CRA’s.
¨(10%) QueryResolution– ensureall databasequeries; sponsors written data queries, CRA monitoringqueriesandinternalQAaudit findings areresolvedwithintheagreedtimelines.
¨(10%) Responsible forensuringtheweeklyData EntrySchedule is updatedandaccurately reflects study workload.
¨(5%) StudyCloseDown-Ensure completedCRF’saresignedbythe Principal or Associate Investigator and that all CRF’s and source data is archived on completion of the study.
¨(5%)Performotherjobrelateddutiesas assigned.
Minimum requirements
Typicallylookingfor1-2yearsofdata handlingexperience.Experiencecanbefroma clinical or non-clinical background. For example financial data handlingbackground.
¨Excellentwrittenandoralcommunicationskills
¨Abilitytoprioritizeworkloads
¨Goodorganizationalskills
¨Previouscustomerserviceexperiencedesirable
Summary:
The main function of a clinical trials assistant is to assist the clinical research teams in ensuring the most effective and efficient conduct by providing administration and project tracking support.
Job Responsibilities:
To provide general administrative support to the Clinical Operations Department and assistance.
To support the Clinical Operations teams with ongoing conduct of studies.
To assist project teams with study specific documentation and guidelines as appropriate. Set up, organize and maintain clinical study documentation.
Process Data Collection Forms i.e. log in, tracking, quality control as appropriate for the study.
Assist in quality control audits of clinical study documentation.
To assist in co-ordination of Investigator payments, if applicable.
To assist in the production of slides, overheads, etc., as needed for project, departmental, sponsor and/or business development presentations.
To assist with the coordination of team member tracking.
Skills:
Verbal and written communication skills, attention to detail, and problem solving skills. Basic ability to work independently and manage ones time. Basic knowledge of the information and techniques needed to diagnose and treat human injuries and diseases. Basic ability to analyze data and accurately document and record results. Education/Experience: High school diploma or GED required. Associate's degree in medical technology or vocational training preferred. 0-2 years experience required