Clinical Research Coordinator
Company: Prisma Health
Location: Greenville
Posted on: April 16, 2024
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Job Description:
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Group","displayCareerSite":true,"jobUpdated":"2024-04-12T00:31:38.125Z","userType":"external","ml_country":"United
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health. Serve with compassion. Be the difference.Job SummaryUnder
minimal supervision, assists with screening, consents, enrollment
and maintaining research subjects as well as maintain compliance to
research protocols. Acts as the liaison between monitors,
investigators and study personnel regarding all data management for
patients enrolled in clinical trials. Responsible for abstraction
of accurate, complete and timely data from the medical record, as
needed. Maintains protocol regulatory documents in compliance with
SOPs. Provides a safe environment for patients, families and
clinical staff.Accountabilities* Independently compiles the medical
records of research subjects during the on-study, treatment and
follow-up periods and reports required elements to the research
sponsor in a complete, accurate and timely manner. Ensures protocol
compliance and accurate data submissions during the treatment and
post treatment phase of a research trial. Ensures that research
tasks are completed correctly by referencing the most current copy
of the research protocol and by accessing the research sponsor
resources to complete tasks. Ensures compliance with regulatory
requirements throughout the study process. Maintains accurate data
on research patients in the research department database. Ensures
medical record accurately reflects research billing
guides.\u00A030%* Develops and maintains a systematic approach to
ensure all research data is reported in the time frame specified by
the protocol. Performs query resolution in a timely manner.
\u00A020%* Performs tasks associated with enrollment and active
treatment period of research subjects. Collects and ships research
specimens, gathers and submits radiological scans, performs
clinical procedures such as EKGs as required by the research
sponsor.\u00A0 Assists in ensuring investigational drugs are
maintained and distributed according to the protocol and FDA
guidelines.\u00A020%* Assists research nurses in screening,
consenting, and re-consenting research subjects. \u00A010%*
Prepares research records and participates in monitor visits or
audit inspections. Participates in protocol specific training
(initiation visits) conducted by the sponsor. Facilitates
communication between the study sponsor, research nurses and
investigators. \u00A020%Supervisory/Management ResponsibilitiesThis
is a non-management job that will report to a supervisor, manager,
director or executive.Minimum EducationAssociate's
Degree-\u00A0Clinical, healthcare or scientific related field
requiredMinimum Experience3 years-\u00A0Allied health, medical or
research related experience\u00A0In lieu of the Above Minimum
RequirementsBS degree in clinical, healthcare or scientific related
field required and 1 yr of experience\u00A0Other Required
ExperienceSoCRA or ACRP certification- PreferredOncology medical
research experience- PreferredSome medical office experience
preferable in oncology- PreferredMedical terminology knowledge-
Preferred\u00A0Work ShiftDay (United States of
America)LocationCancer Centers - Faris RoadFacility1008 Greenville
Memorial HospitalDepartment10557166 Biorepository Services-CIFShare
your talent with us! Our vision is simple: to transform healthcare
for the benefits of the communities we serve. The transformation of
healthcare requires talented individuals in every role here at
Prisma Health.
Keywords: Prisma Health, Greenville , Clinical Research Coordinator, Healthcare , Greenville, South Carolina
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