Clinical Research Coordinator II - Orlando Health Cancer Institute - Urology Research Department

Benefits

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
• •2 more items(s)

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
• •17 more items(s)