Job DescriptionThe University of Maryland, Baltimore (UMB), Institute of Human Virology (IHV)
, is currently recruiting for a Nurse Coordinator
. The Nurse Coordinator will lead clinical research staff in study start up, study conduct and intense nursing studies activities for Clinical Research Unit at the Institute of Human Virology. Benefits Information:
UMB offers a generous benefits package, which includes 22 vacation days, 14 floating and holidays, 15 sick days; comprehensive health insurance and retirement options; and tuition remission for employees and their dependents at any of the University System of Maryland schools. In the Fall of 2021, UMB will require all faculty, staff, and students to be vaccinated against COVID-19. Exemptions for medical or religious reasons will be processed through Human Resources. Primary Duties:
- Leads the activities of one or more research studies and the nurses engaged in research or clinical trials and the provision of health care to research patients. Responsible for overseeing research projects, and ensuring that nurses and staff are aware of study protocols. Develops and tracks work flow policies, recruitment strategy, and progress through the duration of the research study or clinical trial. Collaborates with Principal Investigators and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
- Oversees day to day clinical research operations that require expertise of a Registered Nurse and leads study design, initiation, execution, and completion of clinical trials, research studies, or projects. Ensures compliance of assigned staff with study protocols and overall clinical objectives. Oversees interaction with subject participants including eligibility screening, recruitment, and enrollment. Ensures informed consent is properly secured and documented, counseling, and obtaining patient medical history
- Serves as a patient advocate throughout the research study or clinical trial. Develops and conducts patient and family education. Instructs and counsels patients in research procedures and administers treatment procedures. Oversees patient care in compliance with the research study or clinical trial protocol requirements.
- Performs Institutional Review Board (IRB) and Health Insurance Portability and Accountability Act (HIPAA) protocol development and ensure compliance of research operations with protocols
- Identifies protocol or patient problems, informs investigators of problems, and resolves problems by making protocol modifications or adjustments to care plans. Develops, recommends, modifies, and implements policies and procedures and/or methods of clinical research to meet changing needs and requirements and enforces standards. .
- Obtains biologic tissue and blood samples as necessary and collects information through interviews, questionnaires, test results, and charts. Administers study medications and accurately document the administration in the source document.
- Oversees study and research related documentation development and distribution. Leads the management and analysis of clinical research protocol and data collection of complex research studies or clinical trials.. Develops monitoring plans based upon research protocols in compliance with regulatory agencies. Develops methods for collection, database storage, tracking, analysis, and interpretation of data. Prepares research findings for reports.
- Performs day-to-day operational duties such as: monitoring the budget; budget negotiation and review, ensuring quality control and safety compliance; identifying research opportunities, serving as liaison with IRB, submitting invoicing.
- Identifies and prepares research grants, publications in medical and nursing literature, study materials, brochures, and correspondence.
- Serves as the primary liaison to other departments, outside organizations, government agencies, and sponsor to promote effective and efficient operation and use of resource. Establishes, maintains, and fosters a cooperative relationship between the members of the research team and supports staff by communicating information; responding to requests; building rapport; participation in team problem-solving methods. Oversees the recruitment, performance, scheduling, and training of team members and continually reviews strengths and weaknesses of staff to maintain a well-trained, highly involved, and motivated team. Instruct and train research and nursing staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, and documentation procedures.
- Perform other duties as assigned.
Bachelor's Degree in Nursing or another discipline appropriate to position. Experience:
Five (5) years as Registered Nurse with at least one (1) year in research specialization. Additional years of research preferred. Supervisory Experience:
Current Maryland license in good standing issued by the Maryland Board of Nursing to practice as a registered nurse or a multistate licensure privilege to practice as a registered nurse in Maryland or appropriate federal district licensure where research is conducted. Other:
Certification from Association of Clinical Research Professionals or Society of Clinical Research Associates preferred.
May require training related to occupational safety and health, environmental compliance, shipping of hazardous materials and/or ionizing radiation. Knowledge, Skills, Abilities:
Knowledge of position requirements. Knowledge of all applicable requirements, regulations, and laws. Skill in effective use of applicable technology/systems. Ability to effectively communicate both verbal and written thoughts, ideas, and facts. Ability to work cooperatively with others and independently. Ability to demonstrate, understand, apply, and adhere to the UMB Core Values of Accountability, Civility, Collaboration, Diversity, Excellence, Leadership, and Knowledge. Hiring Range:
Commensurate with education and experience
UMB is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law or policy. For assistance related to employment, please contact the Staffing department at [email protected]
If you anticipate needing a reasonable accommodation for a disability under the Americans With Disabilities Act (ADA), during any part of the employment process, please submit a UMB Job Applicant Accommodation Request. You may also contact [email protected]
Please note that only inquiries concerning an ADA request for reasonable accommodation will be responded to from this email address. Job:
Reg or CII Exempt StaffShift:
School of Medicine - Institute of Human VirologyJob Posting:
Aug 3, 2021Unposting Date: