Clinical Research Coordinator I - Orlando Health - Corporate - Full Time

Position Summary
Participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research.

Seeking individual with a high attention to detail, quick learner, and able to work in a fast-paced environment. Individual must be comfortable working with patient’s and in an operating room setting.

Essential Functions 
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 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.
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. 
Support the team of data managers by answering complex questions and entering information into the EDC if necessary.

Education/Training
Must meet one of the following: 
Bachelor’s 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). 
If no degree, experience may be substituted at a two for one ratio and a minimum of one-year clinical research experience
required.

Licensure/Certification 
All RNs and other Clinical Research Coordinators involved in direct patient care may be required to be licensed by the
medical director. 
BLS/Healthcare Provider certification required.

Experience 
One (1) year of healthcare experience required