Clinical Research Coordinator - RN

Flourish Research•Inverness, FL

28d•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 Clinical Research Coordinator (Registered Nurse) at our Inverness research site location. The Clinical Research Coordinator - RN is responsible for the ethical and accurate coordination and administration of clinical trials under the direction of the Site Manager, the Principal Investigator, and the Medical Director. The CRC will perform diverse administrative and clinical duties requiring analysis, sound judgement, and a high level of knowledge of study-specific protocols, while providing an impeccable patient experience in every, single interaction. Shift: Monday-Friday, 7 AM - 4 PM (occasional weekends) Location: 411 West Highland Boulevard, Inverness, FL 34452 Compensation: Hourly rate based on experience Benefits: Health, dental, and vision insurance plans, 401(k) with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays. Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others! Flourish Research is where clinical trials thrive. Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines. 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 Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. 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! It is the policy of Flourish Research not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, or veteran status.

Requirements

Must be a Registered Nurse (RN) in the state of Florida
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.
High level of integrity and accountability
Abiility to function effetively and positively in a team environment
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
BCLS training required

Nice To Haves

Bachelor’s degree preferred
Associate's degree in nursing or related field preferred
Recommended to sit for Certified Clinical Research Coordinator certification after two years’ experience

Responsibilities

Maintain familiarity with FDA regulations for clinical research
Administratively and clinically manage approximately six to ten clinical trials
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
Other duties as assigned by management