Clinical Research Coordinator: Trials Oversight

Providence Health Plan Group; Orange, Northern (CA, KY); Hybrid; USD 46,000 - 71,000; Full time

Job summary

Providence Health Plan Group is seeking a Clinical Research Coordinator to oversee daily operations of multiple clinical research studies under the supervision of the Medical Office Administrator. You will interface with the Principal Investigator, patients, sponsors, and the IRB to ensure timely and accurate documentation and strict adherence to study protocols (GCP/ICH).

We value a background in medical or phlebotomy training and prefer candidates with vocational schooling, biosafety packaging

Qualifications

• Completion of an accredited Medical or Phlebotomy training program or equivalent educ/experience
• Graduate of a Vocational School or college
• Biohazardous Material packaging training (preferred)
• Phlebotomy certification or equivalent credentials may be required upon hire

Responsibilities

• Oversees day-to-day operations of multiple clinical research studies under the supervision of the Medical Office Administrator
• Interfaces with Principal Investigator, patients, sponsors, and the IRB to ensure timely, accurate documentation
• Ensures strict compliance to study protocols (GCP/ICH) and maintains study documentation quality

Education

Accredited Medical or Phlebotomy training program or equivalent education/experience

Vocational School or college degree

Coursework/Training: Biohazardous Material packaging training

Job description

Providence Health Plan Group is seeking a Clinical Research Coordinator to oversee daily operations of multiple clinical research studies under the supervision of the Medical Office Administrator. You will interface with the Principal Investigator, patients, sponsors, and the IRB to ensure timely and accurate documentation and strict adherence to study protocols (GCP/ICH).

We value a background in medical or phlebotomy training and prefer candidates with vocational schooling, biosafety packaging