Clinical Research Coordinator: The Cancer Institute Faris-FT, Days
Company: Prisma Health
Location: Greenville
Posted on: January 20, 2023
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Job Description:
Inspire 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.30%* 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. 20%* 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. Assists in ensuring investigational drugs are maintained
and distributed according to the protocol and FDA guidelines.20%*
Assists research nurses in screening, consenting, and re-consenting
research subjects. 10%* 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. 20%Supervisory/Management
ResponsibilitiesThis is a non-management job that will report to a
supervisor, manager, director or executive.Minimum
EducationAssociate's Degree-Clinical, healthcare or scientific
related field requiredMinimum Experience3 years-Allied health,
medical or research related experienceIn lieu of the Above Minimum
RequirementsBS degree in clinical, healthcare or scientific related
field required and 1 yr of experienceOther Required ExperienceSoCRA
or ACRP certification- PreferredOncology medical research
experience- PreferredSome medical office experience preferable in
oncology- PreferredMedical terminology knowledge- PreferredWork
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: The Cancer Institute Faris-FT, Days, Healthcare , Greenville, South Carolina
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