Clinical Research Coordinator — Precise, Patient-Focused Trials

Providence Health & Services; Fullerton (CA); On-site; USD 45,460 - 70,257; Full time

Job summary

Providence Health & Services is seeking a Clinical Research Coordinator to manage daily operations of multiple clinical studies and liaise with the PI, patients, sponsors, and IRB. The role emphasizes strict adherence to study protocols and high-quality documentation.

Candidates with experience in clinical research and bilingual English/Spanish communication are preferred, with a background in phlebotomy training and relevant education. Work is on-site in a clinical research setting.

Qualifications

• 2 years of experience in a Clinical Research setting (3 years preferred).
• Bilingual English/Spanish communication skills.
• Completion of an accredited medical or phlebotomy training program or equivalent education/experience.

Responsibilities

• Oversee day-to-day functions of multiple clinical research studies.
• Interface with Principal Investigator, patients, sponsor, and IRB.
• Ensure timely and accurate documentation and strict GCP/ICH protocol compliance.

Skills

Clinical Research experience

Bilingual English/Spanish

Phlebotomy training

Education

Medical/Phlebotomy training program

Vocational/college diploma

Job description

Providence Health & Services is seeking a Clinical Research Coordinator to manage daily operations of multiple clinical studies and liaise with the PI, patients, sponsors, and IRB. The role emphasizes strict adherence to study protocols and high-quality documentation.

Candidates with experience in clinical research and bilingual English/Spanish communication are preferred, with a background in phlebotomy training and relevant education. Work is on-site in a clinical research setting.