Registered Nurse - Clinical Research Coordinator

Work Shift

8 Hours
- Day Shifts (United States of America)

40

Salary Range: $27.50 - $44.00

No

Based on site in Sioux Falls, SD, this role offers the opportunity to build valuable experience in clinical research while working across a variety of studies. You will engage directly with patients, physicians, nurses, and research teams to support each step of the research process.

As a RN Clinical Research Coordinator, you will manage key components of study operations, including outreach, patient recruitment, conducting interviews, answering participant questions, scheduling, and coordinating tests and procedures. Success in this role requires strong communication skills, a collaborative mindset, and a genuine passion for providing excellent patient care.

• Dynamic, supportive team
• Ability to WFH 1x per week after 6 months
• Monday
  - Friday flexible schedule
• Emphasis on employee wellbeing and team building events

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.

• 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 pre-authorization for participants, if applicable.
• Clinical skills may include patient assessment for adverse events and assistance with or completion of study‑related procedures such as injections, phlebotomy, or infusions within state scope of practice.
• Demonstrate a desire and ability to strictly adhere to institutional, state and federal regulations, established research protocols and collaborate with physician investigators to ensure safe and compliant investigational treatment or intervention and follow‑up.
• Attend investigator meetings, coordinate pre‑study site visits and monitor enrollment goals, modifying recruitment plan as needed.
• Ensure 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 follow‑up procedures with potential study subjects.
• Schedule subjects for follow‑up visits to review diaries and questionnaires; ensure appropriate specimen collection, batching and shipping as required.
• Document and maintain all study‑related procedures, processes and events; record protocol deviations and exemptions; maintain accurate source documentation and input data for submission.
• Use appropriate nursing assessment skills to evaluate patient condition in response to study intervention; collect data 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.

• Graduate from a nationally accredited nursing program (e.g., CCNE, ACEN, or NLN CNEA) preferred.
• 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.

If you are an individual with a disability and would like to request an accommodation for help with your online application, please call or send an email to talent.