Clinical Research Coordinator - Bilingual

Flourish Research; Leesburg (FL); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player is seeking motivated and talented individuals to join their team as Bilingual Clinical Research Coordinators. In this role, you will assist in executing clinical research trials while ensuring an exceptional patient experience. This position offers a supportive work environment with opportunities for growth and development. You will engage in various responsibilities, including obtaining informed consent, executing study protocols, and maintaining study-specific files. Join a progressive company committed to diversity and inclusion, where your contributions can truly make a difference in the lives of others.

Benefits

Comprehensive benefits package

Paid overtime for weekend work

401k match

PTO

Qualifications

• Phlebotomy experience is required; EKG or other lab processes preferred.
• 1 year of experience as a Clinical Research Coordinator is preferable.

Responsibilities

• Obtain informed consent from study participants.
• Execute study protocol procedures in an organized manner.
• Communicate with Study Sponsor/CRO regarding study-specific questions.

Skills

Phlebotomy

Excellent communication skills

Organizational skills

Critical thinking

Interpersonal skills

Education

Bachelor's degree

Tools

e-source reporting

Microsoft Office Suite

Job description

Clinical Research Coordinator - Bilingual

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 Bilingual Clinical Research Coordinators at our Leesburg, FL location!

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, single interaction.

Shift: Monday-Friday, 8 AM - 5:00 PM (occasional weekends)

Compensation: Competitive base hourly compensation + comprehensive benefits, PTO, and 401k match

• Paid overtime for weekend work, evening work, or early morning work as needed

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

Qualifications

• Bachelor's degree preferred but not required
• Phlebotomy experience is required, EKG or other patient labs/processes preferred
• Preferably 1 year 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 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.