Clinical Research Specialist

Community Health System•Fresno, CA

1d•$37 - $48

About The Position

The Clinical Research Specialist works closely with the Principal Investigator to facilitate and coordinate daily clinical trial activities. The role supports a range of research, including study testing, enrollment in multicenter clinical trials, and longitudinal cohort studies. It requires careful handling of sensitive information, adherence to study protocols, and maintenance of IRB approval. The specialist contributes to the quality improvement of the research process through study coordination, regulatory compliance, data management, and participant support.

Requirements

Bachelor's degree in a healthcare or health sciences field.
At least 1 year of research or clinical-trial experience.
Obtain one of the following within 1 year of hire or transfer into the position: CRA (Clinical Research Associate) or CCRP (Certified Clinical Research Professional).
Current Basic Life Support (BLS) for Healthcare Providers certification from the American Heart Association (AHA).

Nice To Haves

Master's degree in a healthcare or health sciences field.

Responsibilities

Participate in developing accurate source material for training with other clinical departments as required.
Prepare and maintain IRB documentation, including study applications, modifications, renewals, and closures.
Collect, document, enter, and report data accurately and on time in sponsor and study-specific databases.
Ensure research-site compliance with protocols and regulatory requirements, including appropriate methods, practices, and procedures for research activities.
Ensure compliance with federal, state, and hospital policies and procedures.
Conduct ongoing quality-control audits and maintain investigational drug accountability.
Communicate and collaborate on study requirements with the Principal Investigator, research teams, internal and external parties, sponsors, monitors, and study participants.
Monitor patients for study eligibility and assist potential research participants with the informed-consent process.
Identify and report issues that may affect study design accuracy and quality.