Coordinator in Training

Flourish Research is where clinical trials thrive.

Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status.

We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities.

WESEEYOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

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.
Shift: Monday-Friday day shift (40 hours per week)
Location: Onsite, Jacksonville, FL
FLSA Classification: Non-Exempt

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.

• 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

• Bachelor’s degree preferred

• Associates degree in nursing or related field preferred

• Two years in a related healthcare position

• Pleasant, outgoing,…