Registered Nurse (RN) - Research, Pediatrics, FT
Company: Prisma Health
Posted on: March 12, 2023
Inspire health. Serve with compassion. Be the difference.
Responsible for the implementation, management and oversight of 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.
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%
Evaluates outcomes, interacts, communicates and consults the health care team as required and adjusts nursing care processes as indicated to ensure optimal patient care. - 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 - Interacts with other members of health team to monitor protocol compliance and to ensure that the assigned patient care needs are met. -- 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. - 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. - Reviews records/forms for compliance with protocol requirements. - Prepares for and manages: - pre-site, 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. - 15%
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 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. - 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. -- 5%
Provides functional supervision 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 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%
This is a non-management job that will report to a supervisor, manager, director or executive.
Associate's Degree - Nursing.
1 year - -Nursing experience in a specialty area.
Current SC RN License.
Other Required Sills and Experience
BSN - Preferred
Prior research experience - Preferred
Day (United States of America)
Patewood Outpt Ctr/Med Offices
2507 Upstate Administrative Research Staff
25071000 Upstate Administrative Research Staff - Practice Operations
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. - - - - - - - -
---------------------A place where nurses thrive
At Prisma Health, each of our nurses brings their own unique characteristics to their jobs. But what binds us together is our common commitment to Inspire health. Serve with compassion. Be the difference.---------------
RN sign-on bonus currently available
Now is the perfect time to join Prisma Health if you are an experienced RN with a minimum of 1-year acute care experience and licensed in South Carolina! We offer up to a $30,000 sign-on bonus for eligible full-time positions and $10,000 for part-time positions (minimum of 20 hours per week). Prisma Health requires a one-year commitment (we're confident you're going to love working here). We also offer relocation assistance!
Our team is comprised of nearly 29,000 people helping us change thousands of lives for the better every day.
A strong legacy of care
As South Carolina's largest private, non-profit healthcare system, and second-largest private company, we are here to create a better state of health for South Carolinians. Prisma Health is inspired to help people live their healthiest lives. As the most comprehensive integrated healthcare system in South Carolina, we're on a journey to transform the healthcare experience for our patients and their families.
That's why our team members are dedicated to living our purpose: -Inspire health. Serve with compassion. Be the difference.
Inspire health. Serve with compassion. Be the difference.
Keywords: Prisma Health, Greenville , Registered Nurse (RN) - Research, Pediatrics, FT, Healthcare , Greenville, South Carolina
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