RN Research Nurse Coordinator II - Cardiology

Washington University; Missouri; On-site; USD 65,000 - 110,000; Full time

Job summary

Washington University in Saint Louis seeks an RN Research Nurse Coordinator II in Cardiology to lead a multidisciplinary research team, coordinate enrollment, and ensure protocol adherence. The role includes start-up activities, IRB submissions, budget reviews, and data management.

You will provide direct patient care, screen and enroll subjects, manage study documents, train staff, and monitor safety events, with a commitment to research integrity and participant protection.

Qualifications

• Basic Life Support certification.
• Clinical research certification preferred.
• Experience in academic research setting preferred.

Responsibilities

• Lead and coordinate study enrollment and data collection.
• Ensure protocol compliance and safety reporting as per IRB and sponsor requirements.
• Provide direct patient care and assist physicians in study procedures.
• Train and supervise staff on study activities and data documentation.
• Prepare and submit reportable event reports and study documentation.

Skills

Active Listening

Clinical Research Coordination

Clinical Research Management

Clinical Research Methods

Clinical Research Operations

Clinical Techniques

Detail-Oriented

Effective Written Communication

Oral Communications

Patient Recruitment

Reporting Tools

Team Collaboration

Nursing Fundamentals

Education

Bachelor of Science in Nursing (BSN)

Tools

Electronic Health Records (EHR)

Database Management

Spreadsheet Software

SAS

Job description

## RN Research Nurse Coordinator II - CardiologyApplyremote type: On Campus/Onsitelocations: Washington University Medical Campustime type: Full timeposted on: Posted Todayjob requisition id: JR94037# **Location**SAINT LOUIS, MO 63110# **Scheduled Hours**40# **Position Summary**Functions as the lead person on a research project; coordinates enrollment of study subjects; ensures adherence to study procedures consistent with the study protocol and verifiable source documentation; may supervise personnel assigned to work on the study. Coordinates with multidisciplinary teams to maintain continuity of care and human subject protection with a commitment to research integrity. May perform duties inclusive of those delegated to a Research Nurse Coordinator I.# **Job Description****Primary Duties & Responsibilities:*** Works under the Principal Investigator’s (PI) guidance to meet the research objective of the project.* Facilitates and implements study start-up activities including (but not limited to): trial feasibility assessment; study logistics; IRB (both local and central) submissions and other applicable regulatory requirements; budgetary and contract review and approval.* Provides direct patient care, including assessment, planning, implementation and evaluation of patients; documents, collects data and assists physicians.* Works with research team to identify, screen and enroll study subjects.* Ensures protocol requirements are met including but not limited to: direct contact with research participants; collection of basic health information; coordination of study related procedures; handling, processing and shipping of research specimens, source documentation and data entry.* May train and supervise staff assigned to work on the research project(s).* Coordinates handling of specimens, administration of clinical trials, collection of source information and case reporting.* Prepares/submits reportable event reports to sponsor(s), IRBs and regulatory agencies in accordance with the study protocol and established policies, procedures, and regulations.* Collaborates with sponsor’s research associates during monitoring activities by providing study documentation, data clarifications and reports as necessary.* Authorizes payments to ancillary organizations for services rendered and reconciles payments from organizations serviced.* Demonstrates experience in clinical trials management including strong organizational skills, independence and resourcefulness and an increased responsibility for the day-to-day conduction and oversight of multiple clinical trials.* Provides oversight of administration of study medications and/or study interventions, as appropriate. Administers investigational products in approved settings.* Educates staff nurses caring for research patients by providing necessary information about the research study including intervention and potential adverse events and required study procedures.* Performs other duties incidental to the work described above.**Working Conditions:** Job Location/Working Conditions* Normal office environment* Exposure to blood-borne pathogens* Requires protective devices* Patient care setting* Direct patient care settingPhysical Effort* Typically sitting at desk or table* Typically bending, crouching, stooping* Occasional lifting (25 lbs or less)Equipment* Office equipment* Clinical/diagnostic equipmentThe above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.# **Required Qualifications****Education:**A diploma, certification or degree is not required.**Certifications****/Professional Licenses****:**The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role.Basic Life Support - American Heart Association, Basic Life Support - American Red Cross, Registered Nurse - Illinois Department of Financial and Professional Regulation, Registered Nurse - Missouri Division of Professional Registration**Work Experience:**Related Nursing Or Research (2 Years)**Skills:**Not Applicable**Driver's License:**A driver's license is not required for this position.# **More About This Job****Required Qualifications:*** Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).**Preferred Qualifications:*** Clinical Research Certification.# **Preferred Qualifications****Education:**B.S. - Bachelor of Science - Nursing, B.S.N. - Bachelor of Science in Nursing**Certifications****/Professional Licenses****:**No additional certification/professional licenses unless stated elsewhere in the job posting.**Work Experience:**Academic Research Setting (2 Years)**Skills:**Active Listening, Clinical Research Coordination, Clinical Research Management, Clinical Research Methods, Clinical Research Operations, Clinical Techniques, Database Management, Detail-Oriented, Effective Written Communication, Electronic Health Records (EHR), Nursing Fundamentals, Oral Communications, Patient Recruitment, Reporting Tools, Spreadsheet Software, Statistical Analysis Software (SAS), Team Collaboration# **Grade**S26# **Salary Range**$64,500.00 - $109,900.00 / AnnuallyThe salary range reflects base salaries paid for positions in a given job grade across the University. Individual rates within the range will be determined by factors including one's qualifications and performance, equity with others in the department, market rates for positions within the same grade and department budget.# **Questions**For frequently asked questions about the application process, please refer to our External Applicant FAQ.# **Accommodation**If you are unable to use our online application system and would like an accommodation, please email [e-mail] or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.# **Pre-Employment Screening**All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening.# **Benefits Statement**Personal* Up to 22 days of vacation, 10 recognized holidays, and sick time.* Competitive health insurance packages with priority appointments and lower copays/coinsurance.* Take advantage of our free Metro transit U-Pass for eligible employees.* WashU provides eligible employees with a defined contribution (403(b)) Retirement Savings Plan, which combines employee contributions and university contributions starting at 7%.Wellness* Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more!Family* We offer 4 weeks of caregiver leave to bond with your new child. Family care resources are also available for your continued childcare needs. Need adult care? We’ve got you covered.* WashU covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us.For policies, detailed benefits, and eligibility, please visit: https://hr.wustl.edu/benefits/# **EEO Statement**Washington University in St. Louis is committed to the principles and practices of equal employment opportunity. It is the University’s policy to provide equal opportunity and access to persons in all job titles without regard to race, ethnicity, color, national origin, citizenship (where prohibited by federal law), age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information.