Clinical Research Registered Nurse

Monument Health•Rapid City, SD

1d•Onsite

About The Position

Function as a readily approachable and effective "clinical resource" for the extended clinical research team. Provide clinical leadership through mentorship, education and provide direction for the activities of other research team members. Responsible for the research of and following through on clinical questions which arise. Responsible for the investigation and following through of clinical questions which may arise within areas of focus. Work with administrative, clinical and medical leadership to develop, implement, and facilitate the evolution of systems that ensure adherence to research protocols, institutional policies, local/state/federal regulations, and "Good Clinical Practices". Responsible for the full implementation and management of trials in direct collaboration with administrative and clinical leadership, investigators, sponsors, and clinical research organizations.

Requirements

Completion of a nursing education program that is approved by a board of nursing
Registered Nurse (RN) - South Dakota Board of Nursing
1+ years Registered Nurse
1+ years Clinical Research

Nice To Haves

Bachelors degree in Nursing
Clinical Research Coordinator Certification
Accredited University or accredited training professional; and Human Subject Protection (HSP) - Collaborative Institutional Training Initiative (CITI); and Good Clinical Practice (GCP) - Collaborative Institutional Training Initiative (CITI)

Responsibilities

Coordinates the efforts of case finding and recruitment of study patients.
Discusses protocol participation with patients, completes eligibility forms and assures completion of informed consent.
Identifies educational needs of study patients and their families, providing needed education or resources to meet learning needs.
Utilizes critical thinking in implementing and coordinating medical and nursing interventions.
Initiates interdisciplinary collaboration to assure treatments are administered and modified according to protocol requirements and necessary testing is completed.
Organizes and completes data collection.
Develops forms when needed.
Assists with adverse drug reaction reports.
Responds appropriately to emergency situations, basing patient management decisions on individual patient needs.
Prepares for record reviews and audits with on site teams, FDA, NCI, IRB or other agencies and sponsors when requested.
Initiates interdisciplinary collaboration with clinical trials research team and medical/radiation therapy treatment team to provide access to new treatments when appropriate.
Enhances and documents participation in standard treatments through active navigation of patients/families.
All other duties as assigned.