Clinical Research Coordinator

Flourish Research; San Antonio (TX); On-site; USD 33,062 - 35,817; Full time

Benefits offered by this job

Health, dental, and vision insurance

401(k) with 4% match

Tuition reimbursement

15 days of PTO + 10 company holidays

Job summary

A healthcare research organization in San Antonio is seeking a Clinical Research Coordinator to facilitate participant consent and execute study protocols. Ideal candidates will have phlebotomy experience and strong communication skills, with at least 1 year in a relevant role. This position offers competitive pay and comprehensive benefits, including health insurance and a supportive work environment.

Qualifications

• 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.

Responsibilities

• Obtain study participant informed consent.
• Execute study protocol procedures in a detailed, organized manner.
• Perform human specimen lab draws and processing.

Skills

Phlebotomy experience

Excellent communication skills

Organizational skills

Critical thinking skills

Education

Bachelor's degree (preferred)

Tools

Microsoft Office Suite

Job description

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.

Base Pay Range

$24.00/hr - $26.00/hr

Shift: Monday-Friday, 8 AM - 5:30 PM

Compensation: $24-$26/hr

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.

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 responsibilities as assigned by management.

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!

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.