POSITION SUMMARY

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

EDUCATION/TRAINING

Must meet one of the following:

• Bachelor’s degree in health-related field (i.e., Healthcare Administrative, Nursing, Respiratory Therapy, Health & Wellnessor Health Information Management); or
• Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or HealthInformation Management) and one (1) year of clinical research or healthcare experience (in addition to the requirementslisted in the Experience section); or
• Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in additionto 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 experiencerequired.

EXPERIENCE

• One (1) year of healthcare experience required

Please refer the Job description for details