Inspire health. Serve with compassion. Be the difference.

Job Summary

Accountabilities

• Assists MD to determine patient eligibility for enrollment in research studies.\u00A0 Identifies individual patient needs to facilitate participation including identifying and pre-screening potential participants.\u00A0 Registers patients into research studies to meet protocol parameters.\u00A0 Assists MD investigator in the informed consent process. - 15%

• Evaluates outcomes, interacts, communicates and consults the health care team as required and adjusts nursing care processes as indicated to ensure optimal patient care.\u00A0 Assists MD to monitor patient response to therapy and modify plan of care based upon protocol recommendations; reports changes in patient status and refers appropriate health team members as indicated. - 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\u00A0 Interacts with other members of health team to monitor protocol compliance and to ensure that the assigned patient care needs are met.\u00A0- 10%

• 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.\u00A0 Maintains patient privacy per institutional and study related policies. - 10%

• 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.\u00A0 Reviews records/forms for compliance with protocol requirements.\u00A0 Prepares for and manages:\u00A0 pre-site, study initiation, interim monitoring, and close-out visits.\u00A0 Assists investigator in the completion of data queries.\u00A0\u00A0 Gathers records, reports, lab results, radiographs, scans, and other materials required for institutional, sponsor and FDA audits. - 15%

• Manages study related inventory including, data collection tools, study supplies and study medication, if applicable.\u00A0\u00A0 Schedules visits with the sponsoring agencies. - 5%

• Collaborates with the IRB of record and sponsoring agencies as well as local agencies, when applicable, to ensure global awareness regarding the progression of various studies, amendments and regulatory monitoring.\u00A0 Attends Investigator Meetings as appropriate.\u00A0 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.\u00A0- 5%

• Provides functional supervision over assigned research staff.\u00A0 Ensures assigned study staff practice within the parameters of their qualifications and collaborates with team members for optimal functioning of the unit/department.\u00A0 Trains and oversees staff responsible for data, specimen, and radiology submissions. - 15%

• 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%

• 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%

\u200B

Supervisory/Management Responsibilities

• This is a non-management job that will report to a supervisor, manager, director or executive.

Minimum Requirements

• Associate's Degree - Nursing.
• 1 year -\u00A0Nursing experience in a specialty area.

Required Certifications/Registrations/Licenses

• Current SC RN License.

In Lieu Of The Minimum Requirements Listed Above

• N/A

Other Required Sills and Experience

• BSN - Preferred
• Prior research experience - Preferred

Work Shift

Location

Facility

Department

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.

Inspire health. Serve with compassion. Be the difference.

Job Summary

Accountabilities

• Assists MD to determine patient eligibility for enrollment in research studies.\u00A0 Identifies individual patient needs to facilitate participation including identifying and pre-screening potential participants.\u00A0 Registers patients into research studies to meet protocol parameters.\u00A0 Assists MD investigator in the informed consent process. - 15%

• Evaluates outcomes, interacts, communicates and consults the health care team as required and adjusts nursing care processes as indicated to ensure optimal patient care.\u00A0 Assists MD to monitor patient response to therapy and modify plan of care based upon protocol recommendations; reports changes in patient status and refers appropriate health team members as indicated. - 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\u00A0 Interacts with other members of health team to monitor protocol compliance and to ensure that the assigned patient care needs are met.\u00A0- 10%

• 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.\u00A0 Maintains patient privacy per institutional and study related policies. - 10%

• 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.\u00A0 Reviews records/forms for compliance with protocol requirements.\u00A0 Prepares for and manages:\u00A0 pre-site, study initiation, interim monitoring, and close-out visits.\u00A0 Assists investigator in the completion of data queries.\u00A0\u00A0 Gathers records, reports, lab results, radiographs, scans, and other materials required for institutional, sponsor and FDA audits. - 15%

• Manages study related inventory including, data collection tools, study supplies and study medication, if applicable.\u00A0\u00A0 Schedules visits with the sponsoring agencies. - 5%

• Collaborates with the IRB of record and sponsoring agencies as well as local agencies, when applicable, to ensure global awareness regarding the progression of various studies, amendments and regulatory monitoring.\u00A0 Attends Investigator Meetings as appropriate.\u00A0 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.\u00A0- 5%

• Provides functional supervision over assigned research staff.\u00A0 Ensures assigned study staff practice within the parameters of their qualifications and collaborates with team members for optimal functioning of the unit/department.\u00A0 Trains and oversees staff responsible for data, specimen, and radiology submissions. - 15%

• 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%

• 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%

\u200B

Supervisory/Management Responsibilities

• This is a non-management job that will report to a supervisor, manager, director or executive.

Minimum Requirements

• Associate's Degree - Nursing.
• 1 year -\u00A0Nursing experience in a specialty area.

Required Certifications/Registrations/Licenses

• Current SC RN License.

In Lieu Of The Minimum Requirements Listed Above

• N/A

Other Required Sills and Experience

• BSN - Preferred
• Prior research experience - Preferred

Work Shift

Location

Facility

Department

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.