Clinical Research Coordinator — Growth Path & Impact

Flourish Research

Texas

On-site

USD 33,000 - 36,000

Full time

14 days+

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Benefits offered by this job

Health insurance
Dental insurance
Vision insurance
401k with 4% match
Tuition reimbursement
Parental leave
Referral program
Life insurance
Disability insurance
15 days PTO + 10 company holidays

Job summary

Flourish Research in San Antonio is hiring a Clinical Research Coordinator to assist investigators in executing Phase I–IV trials while ensuring an excellent patient experience. You will obtain consent, perform protocol procedures, manage specimens, and document AE reporting on an e-source system.

The role requires phlebotomy experience, familiarity with ICH/FDA/GCP, strong organizational and communication skills, and at least 1 year of CRC experience.

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 interact with PI, team, sponsors/CROs, and subjects.
  • High-level critical thinking skills.
  • Working knowledge of medical terminology and lab collection/processing/storage procedures.
  • Proficiency with computers and Microsoft Office Suite.

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.
  • Communicate 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.

Skills

Phlebotomy experience
Clinical Research Coordinator
e-source reporting
FDA & GCP regulations
Organizational skills
Interpersonal skills
Microsoft Office

Education

Bachelor’s degree preferred

Tools

e-source platform
MS Office

Job description

Flourish Research in San Antonio is hiring a Clinical Research Coordinator to assist investigators in executing Phase I–IV trials while ensuring an excellent patient experience. You will obtain consent, perform protocol procedures, manage specimens, and document AE reporting on an e-source system.

The role requires phlebotomy experience, familiarity with ICH/FDA/GCP, strong organizational and communication skills, and at least 1 year of CRC experience.

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