Clinical Research Coordinator II - Orlando Health Cancer Institute - Urology Research Department
Behavioral Health Market Context
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Benefits
Orlando Health is committed to providing you with benefits that go beyond the expected, with career-growing FREE education programs and well-being services to support you and your family through every stage of lifeWe begin your benefits on day one and offer flexibility wherever possCareer-growing FREE education programsWell-being services1 more items(s)
Qualifications
- •Bachelor’s degree in health-related field (i.e., Healthcare Administration, 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)
- •If no degree, experience may be substituted at a two for one ratio and a minimum of two years clinical research experience required
- •All RNs and other Clinical Research Coordinators involved in direct patient care may be required to be licensed by the medical director
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Responsibilities
- •Develop, coordinate, and implement research and administrative strategies essential to the management of clinical trials research
- •Work schedule: Monda - Friday, 8:00 am - 5:00 pm
- •Coordinate 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 internal purposes
- •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
- •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
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