Supervisor- Research RN Study Coordinator - CV

Mayo Clinic•Rochester, MN

8h•$88,004 - $132,080

About The Position

Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans – to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. This position will supervise within Cardiovascular Research.

Requirements

Bachelor's degree in nursing required.
Minimum of two years of nursing experience in ambulatory and/or acute care setting.
Completion of Mayo Clinic competency based assessment program will be required within one year of hire.
Ability to adapt to unpredictable situations within clinical and/or research settings.
Excellent verbal and written communication skills.
Strong organizational, interpersonal, and time management skills.
Current RN licensure required for the applicable state.
Basic Life Support certification is required upon hire and must be maintained.

Nice To Haves

SoCRA or ACRP certification preferred.
Previous experience coordinating clinical research studies preferred.
Understanding of basic statistical methods and study design.
Proficiency with spreadsheets, databases, and other software preferred.
Preference given to those who have previous or current experience in cardiovascular research.

Responsibilities

Plans, directs, and coordinates the operational and personnel activities to ensure the provision of high quality care in the research setting.
Promotes ongoing development of all staff and maintains a professional environment.
Functions and is accountable for the RN Clinical Research Coordinator duties.
Independently coordinates complex (i.e. interventional, therapeutic greater than minimal risk) clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
Collaborates with research team to assess feasibility and management of research protocols.
Conducts patient procedures being done for research purposes that require RN licensure (e.g. IV infusions, central line blood draws, etc.).
Performs nursing assessments and patient education, study procedures, medication administration and reconciliation, and monitoring participant status including abnormal lab values, adverse events, disease signs and symptoms and reporting appropriately.
Functions as the nurse coordinator for multiple studies, ensuring that all protocol requirements are met for each enrolled patient.
Responsible for screening and recruitment of eligible patients, patient education and follow-up, preparation of case report forms, accurate protocol documentation, and drug accountability.
Coordinates schedules and monitors research activities and subject participation.
Identifies, reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
Manages, monitors, and reports research data to maintain quality and compliance.
Performs administrative and regulatory duties related to the study as appropriate.
Provides professional nursing care through practice, education, and research.
Educates and serves as a resource for other research personnel.
Collects and assesses data required by the individual protocol and reflective of the patient's status and appropriately interprets information relative to the patient's age-specific needs.
Monitors safety and well-being of study participants.
Some travel may be required.