Sponsor Clinical Research Coordinator (CRA exp preferred)

Category: CRC
Job #: 10876
Utilization: 80%↑
Location: Port St. Lucie, FL area
Job Type: 1099
Therapeutics: No Specific TA Required

We have a unique opportunity for a Coordinator near Port St. Lucie, FL to work onsite for a mock trial with a Device company that's getting ready to launch several regular trials. Must have at least 80% utilization, and it is a big plus to have CRA experience (compensated at a higher rate accordingly). Great potential to transition into the CRA role once the real studies are launched. Must have a minimum 3 years' experience as a fully dedicated regional study coordinator conducting human studies.

Job Responsibilities:

CRC Experience in Medical Device Studies

  • Minimum Clinical Research experience:
    • If no CRA experience - minimum 3 years as a Study Coordinator on human studies.
    • If at CRA experience – minimum of 1 year as a Study Coordinator on human studies.
  • Proven track record as a study coordinator recruiting patients. handling Informed consent, screening eligibility and scheduling visits.
  • Plus:
    • Experience working with or in a startup environment
    • Experience working on medical device or diagnostic studies.
    • Experience working on metabolic studies

Communication Skills

  • Strong verbal communication and active listening skills for conducting pre-screening, screening, and consent processes.

Informed Consent Expertise

  • Familiarity with informed consent processes.
  • Ability to follow detailed protocol to effectively assess patient eligibility and consent capability.
  • Experience in managing minimal-risk studies and explaining associated risks effectively.

Technological Proficiency

  • Competence with data management systems, consent platforms, and other virtual trial tools.

Regulatory Knowledge

  • Understanding of Good Clinical Practice (GCP), HIPAA, and appropriate regulations.

Problem-Solving and Adaptability

    • Ability to handle unexpected challenges and overcome difficulties in reaching and/or recruiting subjects (text, email, phone).
Job Qualifications:
  • Must have a minimum 3 years' experience as a fully dedicated regional study coordinator conducting human studies
  • Must be located within commuting distance of Port St. Lucie, FL
  • Must have at least 80% utilization available
  • Experience with Study Start-up, Medical Device, and Metabolic/Endocrinology studies is a plus
  • CRA experience is a big plus (and will be compensated at a higher rate accordingly)
Apply for this job:

  • Max. file size: 32 MB.
  • This field is for validation purposes and should be left unchanged.