Research Program Coordinator
- Employer
- Johns Hopkins University
- Location
- Maryland, United States
- Salary
- Salary Not Specified
- Date posted
- Apr 21, 2021
View more
- Position Type
- Administrative, Academic Affairs, Research Administration
- Employment Type
- Full Time
You need to sign in or create an account to save a job.
General Summary/Purpose:
Underthedirectsupervision of theClinical Research Program Manager,the Research ProgramCoordinatorisresponsible for monitoringandcollectingresearchdata forcomplementassociateddiseasesin theDivisionofHematology. TheResearchProgramCoordinatorisresponsible forthe organization,entry,maintenanceandaccuracy ofallclinicalresearchdata forcomplexanddetailedclinicaltrials,andmayassistwithorientationoflesssenior researchstaffinprotocolandclinicalresearchinformation.The Coordinator willhelpwithconsenting,collectingresearchsamplesanddeliveringthemto thelab,andhelping topreparemonthly datareportsto thePIandcollaboratinginvestigators.He/She maycollaboratein developmentandwritingofprotocolsandconsentforms, indevelopmentandpreparationof regulatorydocumentsasappropriateandclarifyingconcernsandquestionsaboutnewprotocolswithPIandSponsor.Thisisanintermediate levelposition inmanagingresearchtrialsandregistry databaseswithintheresearchprogram.Specific Duties & Responsibilities:
-
Oversee andconductrecruitment,screeningandenrolling ofeligiblepatients intolaboratoryprotocols.
Explain theprotocolindetailandconductinformedconsentprocedureswithpotentialresearchparticipants.
Maintaingoodworking knowledge ofallassignedprotocolsandreportingrequirements.Work oncomplexclinicalandresearchstudieswhichrequireahighlevelofknowledge,coordination,anddata
abstraction.
Maintainregulatorybinders/spreadsheetsforassignedprotocols.Prepareand submitannualrenewalrequests, amendmentsandadverse eventreportswithclinicalinputaccordingtoIRBandSponsorrequirements.Adheretoallprotocolrequirementstoensurethe validity of
theclinicalresearchdata.
Assisttheprincipalinvestigator andgrant/programmanagerin defininginformationandplansrequiredtoaccomplishgoalsofstudies.Designandcreate protocolspecificcasereportformsasneeded.Assistlessexperiencedstaff indesignandcreationof suchforms.
Verifypatienteligibilityfor studiesbycomparingpatienthistoryandclinicallaboratory
resultswithprotocolrequirements.
Collect,enter andcompile clinicaldatafroma variety ofsources.Ensure accuracyandtimelinessofdatasothatinformationmaybeusedbythephysiciansintreatmentplanningfor individualpatients,andbythePrincipalInvestigatoringrantwritings,presentationsandpublication.
Designandcompile materialswhichaidphysicians/other staffincomplyingwithprotocolrequirements.
MeetregularlywithPrincipalInvestigatortoreview dataaccuracyandoverallstudyprogress.Participateinallmandatorymeetingsto develop
increasingknowledgeofassignedresearch