Nurse Coordinator- Pediatric Neurology

University of Iowa; Iowa City (IA); On-site; USD 60,000 - 80,000; Full time

Job summary

University of Iowa is seeking a Research Nurse Coordinator to manage clinical research protocols, involving patient recruitment, education, data collection, and regulatory compliance. The ideal candidate will possess a Master's degree in nursing or equivalent, a valid Iowa RN license, and at least 1 year of clinical experience. Responsibilities include performing research activities and working with healthcare professionals to ensure study compliance. The position offers a full-time schedule on campus with potential involvement in pediatric patient populations.

Qualifications

• At least 1 year of previous clinical experience.
• 1-3 years’ experience with clinical trials preferred.
• Knowledge of FDA regulations and GCP.

Responsibilities

• Perform clinical research activities and patient visits.
• Educate patients about studies and medication.
• Schedule and conduct trial-related procedures.

Skills

Clinical research activities

Patient education

Data collection and monitoring

Regulatory documentation

Microsoft Office Suites

Education

Master’s degree in nursing

Current Iowa Registered Nurse License

Job description

The research nurse coordinator will apply clinical and administrative skills in carrying out clinical research protocols. The coordinator will be involved in all aspects of research including patient recruitment and enrollment, patient education and assessment, data collection and monitoring, regulatory documentation, and coordination of research visits with all appropriate disciplines. The successful applicant will independently manage one or more primary research protocols, and work closely with other coordinators assisting with related protocols.

Research/Clinical Activities

• Perform clinical/health care research activities.
• Meet with patients during visits.
• Educate patient on scope of study, potential risks and benefits, possible alternatives, and study requirements for patients.
• Review of subject’s medical history.
• Clinical assessment of study participants.
• May administer study medication.
• Educate patients and families about administration and use of study medications.
• Answer patient questions and address concerns between study visits.
• Schedule patient visits within parameters specified to study protocol.
• Assure compliance with study protocol.
• Work closely with a range of health care professionals to carry out study assessments.

Protocol Development And Study Responsibilities

• Assist in protocol development and provide input into descriptions of routine research procedures.
• Assure study visit compliance within window of visit schedule.
• Assist with resolution of monitoring visit issues.
• Serve as liaison to local health care practitioners, agencies, and sponsors.

Subject Recruitment and Enrollment

• Screen for subject eligibility and obtain informed consent for clinical trials/studies.
• Relay information to principal investigator and verify patient eligibility.
• Schedule trial-related procedures and visits.
• Assist with subject assessments during study participation.

Data Collection and Monitoring

• Collect and enter clinical research data required by the sponsors in a timely manner.
• Assist with determining validity of data obtained.
• Maintain detailed record keeping in accordance with clinical research requirements.

Regulatory Guidelines and Documents

• Collect and maintain regulatory documents.
• Prepare regulatory forms and documentation according to protocol requirements.
• Report any reportable events to appropriate party within specified time range.

Human Resources/Leadership

• May provide functional and/or administrative supervision.

Financial Responsibility

• Assist in budget development and monitoring for study.
• Assist in reviewing invoices and work performed before billing.

Education Requirements

• Master’s degree in nursing or a combination of a Bachelor’s degree in nursing and relevant experience.
• A current, valid Iowa Registered Nurse License.

Experience Requirements

• At least 1 year of previous clinical experience.
• Demonstrated experience with Microsoft Office Suites.

Highly Desired Qualifications

• 1-3 years’ experience and participation with clinical trials.
• Knowledge of Institutional Review Board procedures, FDA regulations, GCP and study sponsor guidelines related to clinical trial research.
• Previous experience with Pediatric patient population.
• Experience in clinical trial management including IRB protocols.
• Previous experience with research subject recruitment.
• Previous experience in a role requiring independent decision making.

Additional Information

• Classification Title: Clinical/HC Research Associate
• Appointment Type: Professional and Scientific
• Schedule: Full-time
• Work Modality Options: On Campus

Compensation

• Pay Level: 5A

Contact Information

• Organization: Healthcare
• Contact Name: Natasha Johnson
• Contact Email: [e-mail]

This position is not eligible for University sponsorship for employment authorization.