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Clinical Study Associate - RTD

Dawar Consulting, Inc.
Tucson, USA
Full-time

Ourclient a world leader in life sciences and diagnostics is lookingfor a ClinicalStudy Associate basedoutof TucsonAZ.

Duration : Long term contract (Possibility of furtherextension)

Asa Clinical Study Associate (CSA) within the Clinical ServicesManagement team you will play a crucial role in supporting theClinical Services Project Management Team.

Your primary focus willbe on managing and coordinating tasks related to Sponsorsmonitoring visits and Pharma Partner audits ensuring that allactivities are efficiently executed and compliant with Roche CDxCAP / CLIA Laboratory quality systems.

Your day will involve a rangeof onsite administrative duties designed to keep monitoring visitsand audit requests on Task on Track and onTime.

Responsibilities

  • Coordinateschedules for Study / site Qualification and Initiation VisitsMonitoring Visits Closing Visits and Audits ensuring timely andorganized planning.
  • Maintain andprepare laboratory and study documents for audits includinguptodate Delegation of Authority (DOA) Logs device accountabilitylogs and device registration study binders.

Collaborate with LabManager and / or representative to ensure timely provision ofrequired documentation.

  • Facilitateand / or attend monitoring visits ensuring all activities areconducted smoothly and in compliance with studyrequirements.
  • Complete and managesupplier questionnaires coordinating with Subject Matter Experts toensure timely completion and maintenance ofdocumentation.
  • Participate ininitiatives to enhance processes and improve efficiency within theclinical servicesenvironment.
  • Perform other tasks asassigned by Clinical Services Management demonstrating flexibilityandadaptability.

Education / Skills

  • Bachelors degree in life sciences nursing Business Administration or arelated field; additional qualifications through experience may beconsidered.
  • 2 years inadministrative management entrylevel CRA CTA or a background inhistotechnology laboratories ispreferred.
  • Strong written and verbalcommunication skills in English; proficiency in other languages isa plus.
  • Skilled in Microsoft Office(Word Excel PowerPoint) and GoogleTools.
  • Excellent organizationalabilities with the capability to multitaskeffectively.

CompanyBenefits : Medical Dental Vision Paid Sick leave401K

Ifinterested please send us your updated resume at

Clinical trials

30+ days ago
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