Clinical Research Coord - Day - Full Time - Corp
About The Position
Participate in the development, coordination and implementation of 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 guidance of supervising principal investigators. The coordinator will assess patient eligibility, implement protocol procedures, monitor patient responses, and provide patient education. Additionally, the role requires completing various reports for regulatory agencies and internal purposes, collaborating with healthcare staff to ensure adherence to guidelines, and assisting with protocol amendments and educational in-services. The position also supports interdepartmental cooperation and requires maintaining regular attendance and compliance with organizational policies.
Requirements
- One (1) year of healthcare experience required.
- BLS/Healthcare Provider certification required.
Nice To Haves
- 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.
- All RN’s and other Clinical Research Coordinators involved in direct patient care may be required to be licensed by the medical director.
Responsibilities
- 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 in 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.
- 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.
- Support the team of data managers by answering complex questions and entering information into the EDC if necessary.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
