Clinical Research Coordinator: Drive Multi-Study Trials

Agence PROvidence; Fullerton (CA); On-site; USD 45,000 - 70,000; Full time

Job summary

Providence is seeking a Clinical Research Coordinator in Fullerton, CA to oversee day-to-day operations of multiple studies and ensure all documentation aligns with GCP/ICH protocols. You will collaborate with the Principal Investigator, patients, sponsors and the IRB, maintaining strict compliance and high data quality.

Ideal candidates will have medical or phlebotomy training or 2 years of clinical research experience, plus a high school diploma or GED.

Qualifications

• Completion of an accredited medical or phlebotomy training program or 2 years of clinical research experience.
• High School Diploma or GED or equivalent education/experience.

Responsibilities

• Oversee day-to-day functions of multiple clinical research studies.
• Interface with Principal Investigator, patient, sponsor, and IRB.
• Ensure documentation is timely, accurate and compliant with study protocols (GCP/ICH).

Skills

Medical training

Clinical research experience

Communication skills

Education

Medical or Phlebotomy training program

High School Diploma or GED

Job description

Providence is seeking a Clinical Research Coordinator in Fullerton, CA to oversee day-to-day operations of multiple studies and ensure all documentation aligns with GCP/ICH protocols. You will collaborate with the Principal Investigator, patients, sponsors and the IRB, maintaining strict compliance and high data quality.

Ideal candidates will have medical or phlebotomy training or 2 years of clinical research experience, plus a high school diploma or GED.