RN Clinical Research Coordinator - Oncology Trials
RN Clinical Research Coordinator - Oncology Trials
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Sanford Health is one of the largest and fastestgrowing notforprofit health systems in the United States. Were proud to offer many development and advancement opportunities to our nearly 50000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprint.
Work Shift:
8 Hours Day Shifts (United States of America)Scheduled Weekly Hours:
40Salary Range: $27.50 $44.00Union Position:
NoDepartment Details
MondayFriday schedule 8:00AM4:30PM*No night weekends or holidays*
Summary
Provides an opportunity to learn daily and contribute to treatments of the future. Enthusiasm for learning required along with participation in educating patients physicians nurses and other personnel to the research process.Job Description
Advanced nursing position that involves clinical patient contact research study coordination and study data management. Must be able to organize complex components of clinical trials including test ordering procedure scheduling and insurance preauthorization for participants if applicable.
Clinical skills that may be required include but not limited to: patient assessment for adverse events and assistance with or completion of study related procedures as detailed in the research protocol (ex: injections phlebotomy or infusions) within the applicable state scope of practice.
Demonstrate a desire and ability to strictly adhere to all levels of institutional state and federal regulations and established research protocols and the ability to collaborate with physician investigators to ensure safe and compliant investigational treatment or intervention and followup.
Attend investigator meetings and coordinate prestudy site visits. Monitor enrollment goals and modify recruitment plan as needed. Ensure the completion of all screening eligibility and enrollment procedures. Work with pharmacy to dispense study articles and provide subject education.
Clarify questions and concerns with the investigator and sponsor regarding enrollment goals sponsor expectations and study procedures. Review inclusion/exclusion criteria to assure subject eligibility and review with physician investigator. Review study protocol informed consent form and followup procedures with potential study subjects.
Schedule subjects for followup visits to review diaries and questionnaires. Ensure appropriate specimen collection batching and shipping as required. Document and maintain all studyrelated procedures processes and events. Document protocol deviations and exemptions and record accurate and timely data. Maintain accurate source documentation for all case report entries and input data for submission.
Required to use appropriate nursing assessment skills to evaluate patient condition in response to study intervention. Collect data regarding patient condition for review by the physician investigator.
Prepare case report forms and source documents for sponsor review. Abstract data from medical records clinic consultation and referral notes for preparation of study forms and flow sheets.
Communicate effectively with subjects research team Institutional Review Board (IRB) and sponsor representatives.
Occasional local travel between sites and student supervision may be required.
Qualifications
Graduate from a nationally accredited nursing program preferred including but not limited to Commission on Collegiate Nursing Education (CCNE) Accreditation Commission for Education in Nursing (ACEN) and National League for Nursing Commission for Nursing Education Accreditation (NLN CNEA).Currently holds an unencumbered RN license with the State Board of Nursing where the practice of nursing is occurring and/or possess multistate licensure if in a Nurse Licensure Compact (NLC) state. Obtains and subsequently maintains required department specific competencies and certifications.
Sanford is an EEO/AA Employer M/F/Disability/Vet.
If you are an individual with a disability and would like to request an accommodation for help with your online application please callor send an email to
Required Experience:
IC
Employment Type
Full-Time
