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Clinical Trials Coordinator
at Quest Diagnostics
Seattle, WA

Clinical Trials Coordinator
at Quest Diagnostics
Seattle, WA

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Description

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At Quest, we are on a continuous journey of discovery and\r\ndevelopment. It's this attitude that has made us an industry leader and the #1\r\nDiagnostic Lab in the US. For those joining us, we offer exciting and fast\r\nmoving career opportunities where you can affect change at a rate unheard of in\r\nmany organizations of our size and scope. While we invest in and develop\r\ntechnology to drive our innovations, our ongoing success relies on our people.

As a Clinical Trials\r\nCoordinator, you will work for the world leader in the industry, with a\r\ncareer where you will have the opportunity to collaborate and affect change\r\nwhile expanding your leadership skills and technical knowledge. You can make a\r\nreal impact in a market that is growing and developing.

The Clinical Trials\r\nCoordinator will be based at our Seattle, WA facility.

Clinical Trials Coordinator - the role:

 

The Clinical Trials Coordinator will assist Contract Researchmanagementin all responsibilities related to clinical trials. This requires an awareness of various ongoingclinical trials and their different requirements. This professional will handle themajorityofthe day-to-dayduties related to the clinical trialprojects.

 

The Clinical Trials Coordinator will work with Contract Research management staff on thedrafting, reviewing,or revisingof studyproject SOWs, SOPs, forms andtemplates. This professional will assist in accessioningand trackingstudyspecimens; assembleand send out shippingkits; manage correspondencewith clients and track send back ofmaterials. The Clinical Trials Coordinator will also participate inQA audits and responses.

 

Job responsibilities:

  • AssistProjectManagersinstudymanagementduties

  • Assist in preparingstudyrelated documents and SOPs

  • Providespecimenmanagementsupportincludingaccessioningclinicaltrial specimens,correspondencewithsponsor(s)and/orsitemanagerstoresolvequestions anddiscrepancies

  • Routesamplesfortesting,communicatingwiththeclinicalandresearchbench technologiststoassuretimelycompletionofstudies

  • Signoutcaseswithpathologists,transcribedata,andreportperstudyspecifications

  • Managereturnshipments

  • ArchivestudyslidesandrawdataaccordingtotestingprotocolorSOW

  • Assistwithdataentryand/orauditingofdatainamannercompliantwithDTAof study

  • Documentallprojectsatanappropriatelevel

  • ParticipateinQAaudits andrespondtofindingswhennecessary

  • Participateinmeetings,trainings,committeesandteleconferencesasneeded

  • ParticipateinGLPProjectsincompliancewithTestingProtocolandGLPrequirements

  • SupportthepreparationforsiteQAauditsandassistinthefollowuponaudit recommendations

To qualify, the ideal candidate will have the following skills and experience:

  • Bachelor'sdegreeinBiology,Chemistry,orarelatedscience

  • 2+yearsofexperienceinaclinicallaboratoryorCRO

  • Abilityto manageseveralprojects under supervision

  • Abilityto understand andaddress customer issues andwork with management toensure effective and long-term solutions

  • MTorHTL is preferred

  • Priorpathologyaccessioningexperience is preferred

Apply Today

 

Join us for competitive benefits and development opportunities in a progressive and supportive environment. Help us improve our service, and the experiences of our patients and colleagues. Work with us and together we can be better.

 

Your Quest career. Seek it out.

 

 

 

All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Quest Diagnostics is an Equal Opportunity Employer: Women / Minorities / Veterans / Disabled / Sexual Orientation / Gender Identity.

 

 

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