Clinical Research Coordinator - 225724
📋 Role Overview & Responsibilities
Looking for an entry level Clinical Research Coordinator and an experienced Clinical Research Coordinator to join our team!
Entry Level Clinical Research Coordinator - 6 months - 1 year required Must be comfortable with oncology studies
Experience Level Clinical Research Coordinator - 2 years - 3 years required Must have experience with oncology studies
With assistance, prepares and processes new IRB research proposals, amendments,continuing review applications and adverse event reports according to institutional anddepartmental policies and procedures and federal regulationsPrepares and maintains documents required to be maintained and available internally andfor regulatory authorities and/or the sponsor prior to, during and after the conduct of aclinical/translational trial. Participates in periodic site visits from sponsor, regulatoryauthorities and others to review research, source documentation and research proceduresProcures equipment and supplies needed to fulfill project requirementsRecords data from source documentation and/or participant interaction onto case reportforms (either paper or electronic) with awareness and attention to the requirements foraccuracy, completeness and timeliness. Attends to query resolution in a timely manner.Assures research information is collected and stored in a manner that is compliant withregulations/policies and good clinical practicePerforms packaging and ships study specimens (blood, urine, etc.) to the sponsor orlaboratory in accordance with sponsor and shipping guidelines and regulations, maintainingappropriate documentation
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This position is located in Albuquerque, NM with potential relocation and sponsorship assistance depending on candidate qualifications.
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