CIOS Research Coordinator II, Hematology/Oncology, Full Time, Day
Company: Prisma Health
Location: Greenville
Posted on: May 26, 2023
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Job Description:
Inspire health. Serve with compassion. Be the difference.
Job Summary
Responsible for the implementation, management and oversight of
clinical trial research studies including the education of research
staff, healthcare team member, participants and their caregivers.
Registers, compiles, submits and oversees clinical data, monitors
study compliance and maintains a system for effective data flow for
patients on clinical trials. Manages patient visits and implements
protocol related procedures. Responsible for monitoring and
communicating study participant progress and safety issues with the
investigators, applicable regulatory agencies, health care team and
study staff.
Accountabilities
* Assists MD to determine patient eligibility for enrollment in
research studies. Identifies individual patient needs to facilitate
participation including identifying and pre-screening potential
participants. Registers patients into research studies to meet
protocol parameters. Assists MD investigator in the informed
consent process. 15%
* Provides coordination over assigned research staff. Ensures
assigned study staff practice within the parameters of their
qualifications and collaborates with team members for optimal
functioning of the unit/department. Trains and oversees personnel
managing studies and regulatory matters. 15%
* Collaborates with other health team members to formulate an
interdisciplinary plan of care and plans a schedule of patient
activities related to the study requirements. Instructs
participating health care team members in clinical trials
procedures, and orients health care professionals to the clinical
studies program Interacts with other members of health team to
monitor protocol compliance and to ensure that the assigned patient
care needs are met. 15%
* Identifies specific learning needs and abilities of
patients/families to provide appropriate education at the level of
the recipient. Provides patients/families with information
regarding clinical trial participation and provides education
regarding individual treatment including purpose, potential side
effects, and self-care measures, documents interaction. Maintains
patient privacy per institutional and study related policies.
15%
* Gathers and abstracts study data and documents in a factual,
concise manner which meets regulatory/unit standards. Achieves,
timely, thorough and accurate completion and evaluation of case
report forms. Reviews records/forms for compliance with protocol
requirements. Prepares for and manages: presite, study initiation,
interim monitoring, and close-out visits. Assists investigator in
the completion of data queries. Gathers records, reports, lab
results, radiographs, scans, and other materials required for
institutional, sponsor and FDA audits. 10%
* Manages study related inventory including, data collection tools,
study supplies and study medication, if applicable. Schedules
visits with the sponsoring agencies. 5%
* Collaborates with the GHS IRC (Institutional Review Committee)
and sponsoring agencies as well as local agencies, when applicable,
to ensure global awareness regarding the progression of various
studies, amendments and regulatory monitoring. Attends Investigator
Meetings as appropriate. Prepares and presents lectures and/or
written materials for health care provider education and
participates in presentations or seminars related to the research
study when necessary. 10%
* Assists department manager/supervisor to coordinate resources to
appropriately conduct the trial including the development of data
collection tools, communication with ancillary departments to
implement study related procedures. Collaborates with study team to
develop new strategies for the growth of the Research program.
Communicates study related issues with research management. 5%
* Assists investigator in the development of investigator initiated
research studies including the development of protocols, literature
searches, and data collection tools as well as assistance in the
submission of investigator initiated studies to the IRC and
sponsoring agencies, if applicable. 5%
* Maintains professional growth and development through seminars,
workshops, in-service meetings, current literature and professional
affiliations to keep abreast of latest trends in field of
expertise. 5%
Supervisory/Management Responsibilities
This is a non-management job that will report to a supervisor,
manager, director or executive.
Minimum Education
Other - Associate degree in Allied Health OR Bachelor's Degree in
health sciences or business.
Minimum Experience
1 Year - Research experience in at least one of the following
areas: pharmaceutical, academic, device, NIH, investigator
initiated studies or registry trials.
Specific Acceptable Credentials (if applicable)
If Allied Health Degree: South Carolina certification/license in
field.
In lieu of the Above Minimum Requirements
The following requirements will also be considered in lieu of 1
year research experience:
Associate Degree in Allied Health plus 3 years direct experience in
that field
OR Bachelor Degree in a science and 3 years direct experience in
that field.
In lieu of an Associates or Bachelors degree, 3 years of research
experience or 5 years related experience will be considered.
Other Required Experience
International Air Transport Association Certification -
Preferred
Work Shift
Day (United States of America)
Location
Cancer Centers - Faris Road
Facility
1008 Greenville Memorial Hospital
Department
10559045 Hematology/Oncology-CIF
Share 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 , CIOS Research Coordinator II, Hematology/Oncology, Full Time, Day, Healthcare , Greenville, South Carolina
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