Participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research.
Participate in the coordination of multi-site or large-scale clinical trials research studies conducted by a supervising principal
investigator(s) in support of activities that meet objectives of assigned research protocol(s).
Assesses patients for protocol eligibility and communicates findings to investigator/physician.
Coordinates the implementation of protocol procedures.
Operates specialized equipment as needed in assigned area, if applicable.
Assesses and monitors patient responses and adverse reactions; reports same to accountable sources.
Provides appropriate patient and family education.
Completes a variety of reports, documents and correspondence for regulatory agencies, participating clinical trial sites and for
Collaborates with physicians and other healthcare staff to ensure adherence to FDA and protocol guidelines; identify potential
problems and/or inconsistencies and take action as appropriate.
Assist in the preparation and submission of amendments to clinical trials protocols to the IRB.
Provides educational in-services as needed.
Promotes interdepartmental cooperation and coordination for each protocol.
Maintains reasonably regular, punctual attendance consistent with Orlando Health policies, the ADA, FMLA and other federal, state and local standards.
Maintains compliance with all Orlando Health policies and procedures.
Other Related Functions
Assists in the development of treatment orders for active studies, to be reviewed by the treating physician.
Assists the research team in preparing for site audits.
Attends appropriate departmental and/or corporate meetings
Attends study group and investigator meetings as required.
Demonstrates ability in using computer software specific to department.
Must meet one of the following:
Bachelor degree in health related field (i.e. Healthcare Administrative, Nursing, Respiratory Therapy, Health & Wellness or Health
Information Management) ; or
Associate degree in related field (i.e. Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health
Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in
the Experience section); or
Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the
requirements listed in the Experience section).
All RNs and other Clinical Research Coordinators involved in direct patient care may be required to be licensed by the medical
BLS/Healthcare Provider certification required.
One (1) year of clinical research or healthcare experience required.
Orlando Health is one of Florida's most comprehensive private, not-for-profit healthcare systems providing access to nearly two million Central Florida residents and has provided care for more than 4,600 international visitors annually. Our physician practices, diagnostic centers, hospitals and advanced medical treatments and procedures, along with our highly qualified team of medical specialists, have distinguished Orlando Health as a healthcare leader. We are one of Central Florida's largest employers with more than 15,000 employees and nearly 3,000 affiliated physicians supporting our philosophy of providing a continuum of care that revolves around patients' needs. As a leading healthcare resource, providing world-class medical care as well as training our future healthcare providers, Orlando Health will continue to foster growth and development throughout the region for generations to come. We are looking for talented individuals to be part of our team.
Posting ID: 611339329Posted: 2021-03-09Job Title: Clinical Research Coord