Clinical Research Coordinator II - Med Ed Clinical Research
First - req11433
The Clinical Research Coordinator II develops, coordinates and implements research and administrative strategies essential to the management of clinical trials research.
Must meet one of the following:
Bachelor 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).
All RNs and other Clinical Research Coordinators involved in direct patient care may be required to be licensed by the medical director.
Maintains current Certified Research Coordinator CCRC/CCRP by the Association of Research Professionals or SOCRA (Society of Clinical Research Associates.
BLS/Healthcare Provider certification required.
Two (2) years of clinical research experience
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.
About Orlando Health
Orlando Health is a $3.8 billion not-for-profit healthcare organization and a community-based network of hospitals, physician practices and outpatient care centers across Central Florida. The organization is home to the area's only Level One Trauma Centers for adults and pediatrics, and is a statutory teaching hospital system that offers both specialty and community hospitals. More than 3,100 physicians have privileges across the system, which is also one of the area's largest employers with more than 20,200 employees who serve more than 97,000 inpatients, more than 2.5 million outpatients, and more than 4,800 international patients each year. Additionally, Orlando Health provides more than $360 million in total value to the community in the form of charity care, community benefit programs and services, community building activities and more. Additional information can be found at www.orlandohealth.com.