Clinical Trials Lead & Compliance Coordinator

The CORE Institute

Phoenix (AZ)

On-site

USD 60,000 - 85,000

Full time

3 days ago
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Job summary

The CORE Institute in Phoenix, AZ is seeking a Clinical Research Coordinator to oversee and coordinate clinical studies involving human subjects. You will assist with protocol development, regulatory submissions, and ensure compliance with SOPs and regulations while supporting study teams.

You will recruit participants, obtain informed consent, collect data, manage case report forms, and coordinate tests and visits.

Qualifications

  • Bachelor's degree AND three years of clinical trial experience OR Associates Degree AND Certified Clinical Research Coordinator
  • Four plus years experience in the health care field or an equivalent combination of education and experience.
  • Certified Clinical Research Coordinator preferred
  • Knowledge of clinical research regulatory guidelines and regulations

Responsibilities

  • Assist with protocol development and feasibility assessment.
  • Prepare regulatory submissions and manage documentation for assigned studies.
  • Recruit study participants through referrals or ads.
  • Schedule visits, screen and obtain informed consent from potential participants.
  • Collect, monitor and analyze data for research projects.
  • Complete case report forms and document data in study records.
  • Coordinate laboratory tests, imaging studies and exams.
  • Educate patient care teams on study protocols and procedures.

Skills

Clinical trials
Regulatory compliance
Data collection
Communication

Education

Bachelor's degree
Certified Clinical Research Coordinator

Tools

EDC systems
CRF management

Job description

The CORE Institute in Phoenix, AZ is seeking a Clinical Research Coordinator to oversee and coordinate clinical studies involving human subjects. You will assist with protocol development, regulatory submissions, and ensure compliance with SOPs and regulations while supporting study teams.

You will recruit participants, obtain informed consent, collect data, manage case report forms, and coordinate tests and visits.

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