Coordinator in Training

Flourish Research•Jacksonville, FL

2d•Onsite

About The Position

Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. We are actively hiring a Coordinator in Training to support our Jacksonville, Florida site. The Clinical Research Coordinator (CRC) in Training works directly under a Clinical Research Coordinator and is responsible for the ethical and accurate coordination and administration of clinical trials under the direction of the Clinical Research Coordinator, Site Manager, the Principal Investigator and the Medical Director. The CRC in Training will perform diverse administrative and clinical duties requiring analysis, sound judgement, and a high level of knowledge of study specific protocols. A coordinator new to research should be considered a Research Coordinator in Training up to their first two years of experience.

Requirements

Bachelor’s degree preferred
Associates degree in nursing or related field preferred
Two years in a related healthcare position
Pleasant, outgoing, and mature.
Good communication and time management skills.
Attention to detail.
Self-disciplined and motivated.
Diligent and persistent.
Ability to function effectively and positively in a team environment
High level of integrity and accountability
Must have the ability to establish and maintain good working rapport with study patients, physicians, investigators, referring physicians, research staff and clinic
Must exhibit accurate, complete, legible and timely use of communication methods
Familiar with medical terminology
BLS training required

Nice To Haves

Recommended to sit for Certified Clinical Research Coordinator certification after two years’ experience

Responsibilities

Obtain familiarity with FDA regulations for clinical research
Administratively and clinically manage protocols under supervision of CRC
Adhere to company Standard Operating Procedures, Good Clinical Practice and study protocols
Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
Obtain Informed Consent from study participants and verify documentation
Screen potential study participants for inclusion/exclusion criteria
Schedule and conduct study visits per protocol requirements, including but not limited to the following: Dispense study medication in a professional and accountable manner, Collect, process, and ship blood/urine specimens, Perform ECGs, obtain vital signs, Administer questionnaires/diaries
Complete source documentation and maintain timely completion of case report forms
Ensure prompt reporting of events to sponsor and IRB
Assess participant’s condition and report any significant variations from baseline measurements to Principal Investigator
Submit timely patient reimbursement requests to financial team for patient’s participation in protocol
Ensure the filing and maintenance of all regulatory documents
Schedule and prepare for monitoring visits
Maintain communication with Principal Investigator, Sub Investigators, Assistants, sponsors, IRB