Clinical Trial Assistant 9375

This is a contract job opportunity. potential for permPosition : Clinical Trial Assistant 9375Location : Madison WISchedule : 1 CTA rotating between

AM / PM / NOCs,

2 CTA only overnightProjected duration : 6 months + potential for permJob code : CVDJP00029375 Pay rate - $21 to $24 per hour Benefits are available Multiple openingsAccuratelyperformbloodpressure,venipuncture,weights,pulse,respiratoryrate,and temperature readings

Preparationandaccuraterecordingof ECGs / Holters

Collectionandprocessingofbiologicalsamplesasspecifiedintheprotocolandensuresthe proper distribution of those samples

Monitorsmealstoensuredietarycompliancebyresearchparticipants

Assist in the preparation of rooms and medical equipment

Assistwithscreeningproceduresasneeded

Maintainaclean,safeandefficientworkingandstudyenvironment

Foster respectful relationships with study participants

Accuratelyrecordallresearchdataobtainedorobserved

AssistwithQCofsourcedocumentsandcasereport forms

Maintainsabasicunderstandingofcurrentregulatoryrequirements

Attends all required meetings, as appropriate

Assist,asnecessary,withstudyprocedures

Maintainsaccuraterecordsofallworkundertaken

Maintainsskillstoperformallstudytasks,asrequired

Maintainsconstantawarenessofparticipantsafetyanddignityatalltimes

Handlesparticipantcomplaintsefficientlyandeffectivelyinorderthattheirsatisfactionis maintaine

Ensuresthatclientandparticipantconfidentialityismaintained

Responds to client and team queries in a timely manner

Takesownershipforthequalityandstandardofownwork

Observestudysubjectsforgeneralwell-beingandreportappropriately

Check in and check out study participants, as requested

Otherduties as assigned

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 :

HighSchoolDiplomaor equivalent

EMT,Phlebotomy,CMAorCNAcertification,preferred

High school diploma or GED required.Associate's degree in medical technology or vocational training preferred.0-2 years experience required.