Clinical Research Coordinator

Flourish Research; Winter Park (FL); On-site; USD 34,000 - 48,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401k with 4% match

Tuition reimbursement

Parental leave

Referral program

Employee assistance program

Life insurance

Disability insurance

15 days of PTO + 10 company holidays

Job summary

A leading clinical trial company in Winter Park, FL is seeking a Bilingual Clinical Research Coordinator to assist in clinical trials while ensuring an impeccable patient experience. Ideal candidates should have phlebotomy experience and excellent communication skills. You will be responsible for obtaining informed consent, executing study protocols, and performing lab draws. Flourish Research offers a competitive benefits package in a supportive environment, promoting professional growth and excellence in patient care.

Qualifications

• 2+ years of experience as a Clinical Research Coordinator preferred.
• Experience with e-source reporting is a plus.
• Understanding of ICH, FDA, and GCP regulations is necessary.
• 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 interact with the PI, study team, and sponsors.
• Ethical, self-driven with high-level critical thinking.
• Working knowledge of medical terminology and lab procedures.
• Proficiency with computers and Microsoft Office Suite.

Responsibilities

• Obtain study participant informed consent.
• Execute study protocol procedures professionally.
• Perform human specimen lab draws and processing.
• 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.

Skills

Phlebotomy experience

Critical thinking

Excellent communication

Organizational skills

Interpersonal skills

Familiarity with medical terminology

Medical terminology knowledge

Team collaboration

Education

Bachelor's degree preferred

Tools

Microsoft Office Suite

Job description

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.