Research Nurse / Study Coordinator II

University of Florida•Gainesville, FL

5d•$60,000 - $80,000•Onsite

About The Position

The UF Health Cancer Institute is the 72nd NCI designated cancer center and the only one at a public university in the State of Florida. As a matrix cancer center, we span all of the University of Florida's 16 colleges, pulling together a world-class, multi-disciplinary membership of over 350 faculty and 150 staff to address the challenges of the cancer burden faced by the population we serve as we work together to find a cure. As a Study Coordinator II / Research Nurse at the UF Health Cancer Institute (UFHCI), you will be responsible for collaborating with coordinators and research staff, investigators, physicians, nurses, and other key personnel in the clinics, hospitals, and at the Cancer Center to ensure compliance with protocol requirements and satisfactory care for patients enrolled on research protocols.

Requirements

Study Coordinator II: Bachelor’s degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
Research Nurse: Graduate of a nationally accredited nursing program and three years of professional nursing experience.
Licensed as a registered nurse in accordance with Chapter 464, Florida Statutes, or ability to obtain Florida licensure within 3 months of hire.
For both classifications, professional clinical research and/or oncology certification (through SOCRA, ACRP, etc.) are required at the earliest of 12 months from hire or eligibility.
Study Coordinator II: Bachelor’s degree in Health Care, Basic Sciences, or related field
Study Coordinator II: Four (4) to six (6) years of relevant experience and/or training in clinical research, research coordination, and/or oncology preferred
Study Coordinator II: Extensive experience with research databases and/or subject-level data management
Study Coordinator II: Proficiency in Microsoft Office Suite
Study Coordinator II: Strong experience with research databases and data entry/management systems
Study Coordinator II: Excellent time management and ability to manage multiple priorities
Study Coordinator II: Strong attention to detail and accuracy in data and documentation
Study Coordinator II: Ability to maintain confidentiality and handle sensitive research information appropriately
Research Nurse: Master’s degree in Nursing, Health Care, Basic Sciences, or related field
Research Nurse: Six (6) to eight (8) years of relevant experience and/or training in clinical research or oncology
Research Nurse: Extensive experience with research databases and/or subject-level data management
Research Nurse: Professional certification in clinical research (SOCRA or ACRP) and/or oncology certification (OCN or equivalent)
Research Nurse: Proficiency in Microsoft Office Suite
Research Nurse: Strong knowledge of clinical research processes and regulatory requirements
Research Nurse: Experience with clinical research databases and data management systems
Research Nurse: Excellent organizational and documentation skills
Research Nurse: Strong ability to manage complex clinical and research workflows

Nice To Haves

Study Coordinator II: Experience in oncology research and/or clinical trials coordination
Study Coordinator II: Forward-thinking mindset with ability to meet deadlines in a fast-paced environment
Study Coordinator II: Strong ability to build and maintain effective working relationships with diverse stakeholders
Study Coordinator II: Highly resourceful team player with ability to work independently when needed
Study Coordinator II: Strong written communication, organization, and professionalism
Study Coordinator II: Strong interpersonal and communication skills
Study Coordinator II: Ability to collaborate with investigators, physicians, clinical staff, sponsors, and external partners
Study Coordinator II: Strong emotional intelligence and adaptability in dynamic environments
Study Coordinator II: Excellent delegation and prioritization skills
Study Coordinator II: Strong customer service orientation
Research Nurse: Experience in an academic medical center or cancer center research environment
Research Nurse: Forward-thinking, highly accountable professional with ability to meet high-performance goals
Research Nurse: Strong ability to build and maintain effective relationships across multidisciplinary teams
Research Nurse: Highly professional, discreet, and independent with strong teamwork orientation
Research Nurse: Strong written communication and organizational skills
Research Nurse: Strong interpersonal and leadership skills within clinical/research teams
Research Nurse: High emotional intelligence and ability to work in complex clinical environments
Research Nurse: Ability to manage confidential information with discretion
Research Nurse: Strong adaptability in managing competing priorities
Research Nurse: Strong commitment to high-quality customer and stakeholder service

Responsibilities

Coordinating relevant care and protocol required testing for subjects enrolled on an assigned portfolio of human clinical trials.
Interpreting and collecting medical and clinical data for prospective and existing enrolled subjects on assigned clinical trials.
Maintaining compliance with all internal and external regulatory and institutional requirements related to your trials.
Coordinating sample collection, analysis, and shipping for assigned trials.
Subject care and navigation for enrolled subjects including: Facilitating appointments, consults, and data abstraction prior to visits.
Coordinating treatment plans with investigators, clinicians, and other related staff in the clinics.
Communicating test results and findings, clarifying and counseling where needed/appropriate.
Aids subjects and their families in navigating the healthcare systems as related to their treatment.
Serving as point of contact for subjects and their healthcare team.