Flourish Research
Bilingual Clinical Research Coordinator – Winter Park, FL
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.
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every interaction.
Location:
1788 W Fairbanks Ave Suite A, Winter Park, FL 32789
Compensation:
Competitive hourly base compensation
Benefits:
Health, dental, and vision insurance plans, 401k with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays.
Responsibilities
The Clinical Research Coordinator (CRC) obtains study participant informed consent.
Executes study protocol procedures in a detailed, organized, and professional manner.
Performs human specimen lab draws and processing, and packages specimen shipments.
Creates and completes study source documents and adverse event reporting on an e-source system.
Maintains study‑specific files and supplies.
Communicates with the Study Sponsor/CRO regarding study‑specific questions.
Participates in site visits from Sponsors/CROs, including site initiation and monitoring visits.
Additional duties as assigned by management.
Qualifications
Bachelor's degree preferred, but not required.
Phlebotomy experience is required; EKG or other patient labs/processes preferred.
Preferably 2+ years of experience as a Clinical Research Coordinator.
Familiar with e‑source reporting via an electronic platform.
A clear understanding of ICH, FDA, and GCP regulations.
Impeccable organizational skills and attention to detail.
Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.
An ethical compass that compels the candidate to be honest, detail‑oriented, and self‑driven.
High‑level critical‑thinking skills.
Working knowledge of medical terminology and lab collection/processing/storage procedures.
Proficiency with computers and Microsoft Office Suite.
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 is one of the industry’s most progressive and diversified clinical trial companies with robust capabilities in cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from underrepresented groups to help make this vision a reality. We are committed to a safe work environment where all employees, customers, and patients are included, treated with dignity and respect, and celebrated.
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.
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The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every interaction.
Location:
1788 W Fairbanks Ave Suite A, Winter Park, FL 32789
Compensation:
Competitive hourly base compensation
Benefits:
Health, dental, and vision insurance plans, 401k with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays.
Responsibilities
The Clinical Research Coordinator (CRC) obtains study participant informed consent.
Executes study protocol procedures in a detailed, organized, and professional manner.
Performs human specimen lab draws and processing, and packages specimen shipments.
Creates and completes study source documents and adverse event reporting on an e-source system.
Maintains study‑specific files and supplies.
Communicates with the Study Sponsor/CRO regarding study‑specific questions.
Participates in site visits from Sponsors/CROs, including site initiation and monitoring visits.
Additional duties as assigned by management.
Qualifications
Bachelor's degree preferred, but not required.
Phlebotomy experience is required; EKG or other patient labs/processes preferred.
Preferably 2+ years of experience as a Clinical Research Coordinator.
Familiar with e‑source reporting via an electronic platform.
A clear understanding of ICH, FDA, and GCP regulations.
Impeccable organizational skills and attention to detail.
Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.
An ethical compass that compels the candidate to be honest, detail‑oriented, and self‑driven.
High‑level critical‑thinking skills.
Working knowledge of medical terminology and lab collection/processing/storage procedures.
Proficiency with computers and Microsoft Office Suite.
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 is one of the industry’s most progressive and diversified clinical trial companies with robust capabilities in cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from underrepresented groups to help make this vision a reality. We are committed to a safe work environment where all employees, customers, and patients are included, treated with dignity and respect, and celebrated.
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.
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