About Us:
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. WE SEE YOU. 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.
About the Job:
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
Position Summary:
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.
Duties and 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
Requirements
Education and Experience:
Bachelor’s degree preferred
Associates degree in nursing or related field preferred
Two years in a related healthcare position
Qualifications and Requirements:
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…