Position Details
Active - Benefit Eligible and Accrues Time Off Work Hours per Biweekly Pay Period: 80.00
Shift: Monday - Friday
Location: Hollis Cancer Center
Pay Rate: Min $79,164.80 Mid $95,243.20Position Summary
This position will work with staff/faculty to develop, implement, and coordinate projects as assigned by LRH leadership. The research coordinator supports, facilitates, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Position Responsibilities
People At The Heart Of All We Do- Fosters an inclusive and engaged environment through teamwork and collaboration.
- Ensures patients and families have the best possible experiences across the continuum of care.
- Communicates appropriately with patients, families, team members, and our community in a manner that treasures all people as uniquely created.
Safety And Performance Improvement- Behaves in a mindful manner focused on self, patient, visitor, and team safety.
- Demonstrates accountability and commitment to quality work.
- Participates actively in process improvement and adoption of standard work.
Stewardship- Demonstrates responsible use of LRH's resources including people, finances, equipment and facilities.
- Knows and adheres to organizational and department policies and procedures.
Standard Work: Clinical Research Coordinator RN- Supports the development of planning for the study, implementation, and manage day-to-day operations of research programs.
- Translate planning and design decisions into concrete activities and tasks, assign these tasks, and set priorities for their implementation.
- Ensure proper communication among stakeholders, staff, study sponsors, and investigators, to coordinate the assigned directives and accomplish deliverables. The work includes monitoring and coordinating research project operations, including project plans, timelines, and tasks.
- Coordination of staff, faculty, and volunteers in regard to research projects, ensuring that daily tasks are completed, and project timelines are communicated across the team and met.
- Develop project/work plan. Monitor progress, identify and resolve barriers to progress, and work with project leadership to make any necessary adjustments to scope, timeline, and/or budget.
- Coordinate data collection activities including conducting interviews; coordinating survey printing, online survey creation, and distribution; creating and maintaining project timelines; facilitating participating site intervention activities and maintaining contact with sites; recruiting research participants; and coordinating with electronic health records (EHR) and information technology (IT) development staff.
- Deliver safe nursing interventions in an organized, efficient, and prioritized manner under the direction of the clinical trial protocol and PI.
- Administer protocol medications as needed and coordinate with specialized nursing departments to insure protocol adherence.
- Maintaining project compliance with research regulations including creating and renewing IRB protocols, serving as custodian for human subjects' payments, and managing budgets.
- Maintains the Delegation of Authority Log and Training logs, ensuring that all staff have received updated training.
Competencies & Skills
Essential:
- Excellent written and oral communication skills.
- Ability to work independently with minimal supervision.
- Ability to manage multiple projects simultaneously.
- Ability to complete applicable CITI training.
- Strong computer skills (MS Office, including Word, Excel).
Nonessential:
- Familiarity with EHR: Cerner, EPIC, Allscripts, Mosaic.
Qualifications & Experience
Essential:
Nonessential:
Essential:
- Bachelor of Science in Nursing
Other information:
Experience Essential:
- Minimum of 2 years RN exp. or oncology experience or clinical research experience.
Certification Essential:
- ACRP certified or plan to become certified in 2 years of employment.
License Essential:
- Valid RN license in the State of FL.
