Clinical Research Coordinator II - Orlando Health Cancer Institute

Orlando Health•Orlando, FL

18h

About The Position

Orlando Health Cancer Institute is seeking a Clinical Research Coordinator II to develop, coordinate, and implement research and administrative strategies essential to the management of clinical trials research. This role involves coordinating multi-site or large-scale clinical trials research studies under the supervision of principal investigator(s) to meet the objectives of assigned research protocols.

Requirements

Minimum of (1) year clinical research experience.
Must be eligible for Certified Research Coordinator CCRC/CCRP by the Association of Research Professionals or SOCRA (Society of Clinical Research Associates within one year of hire.
BLS/Healthcare Provider certification required.

Nice To Haves

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 Healthn 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.

Responsibilities

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).
Assess patients for protocol eligibility and communicates findings to investigator/physician.
Coordinate the implementation of protocol procedures.
Operate specialized equipment as needed in assigned area, if applicable.
Assess and monitor patient responses and adverse reactions; reports same to accountable sources.
Provide appropriate patient and family education.
Complete a variety of reports, documents, and correspondence for regulatory agencies, participating clinical trial sites and for internal purposes.
Collaborate 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.
Provide educational in-services as needed.
Promote interdepartmental cooperation and coordination for each protocol.
Maintain reasonably regular, punctual attendance consistent with Orlando Health policies, the ADA, FMLA and other federal, state, and local standards.
Maintain compliance with all Orlando Health policies and procedures.
Assist in the development of treatment orders for active studies, to be reviewed by the treating physician.
Assist the research team in preparing for site audits.
Attend appropriate departmental and/or corporate meetings.
Attend study group and investigator meetings as required.
Demonstrate ability in using computer software specific to department.