Clinical Research Coordinator Fort Myers South Fl

U.S. Renal Care

Fort Myers, FL, US
On-site
Coordinate daily clinical trial activities
Ensure informed consent process compliance
Maintain source records and documentation
U.S. Renal Care is seeking a Clinical Research Coordinator in Fort Myers, FL, to oversee daily clinical trial activities in collaboration with a principal investigator and other stakeholders. The role involves ensuring compliance with research protocols and regulations, participant safety, and effective communication among the research team

Job Summary

  • The Clinical Research Coordinator is responsible for coordinating all aspects of participant care from screening through study completion in accordance with the study protocol.
  • The role requires ensuring strict adherence to FDA, ICH, and state regulations while protecting the rights, safety, and welfare of all study participants.
  • The position involves maintaining essential documents, managing patient stipend payments, and collaborating with principal investigators, sponsors, and IRBs to ensure trial success.

Matching Summary

Match Score: 85

U.S. Renal Care is seeking a Clinical Research Coordinator in Fort Myers, FL, to oversee daily clinical trial activities in collaboration with a principal investigator and other stakeholders. The role involves ensuring compliance with research protocols and regulations, participant safety, and effective communication among the research team.

Skills & Requirements

Must-have

  • Coordinate daily clinical trial activities
  • Ensure informed consent process compliance
  • Maintain source records and documentation
  • Report adverse events and protocol deviations
  • Adhere to FDA and ICH regulations
  • Manage investigational product dispensing
  • Protect participant confidentiality under HIPAA

Nice-to-have

  • Patient-care culture emphasis
  • Effective relationship building skills
  • Team concept participation
  • Customer service standards promotion
  • Training and oversight capabilities

Key Requirements

  • Knowledge of Good Clinical Practice (GCP)
  • Understanding of FDA Federal Code Regulations
  • Familiarity with HIPAA Privacy Rule
  • Ability to travel between facilities
  • Maintenance of industry standard licensures

Work Rights

Not specified

Tailored Resume

Cover Letter