Clinical Research Spec.

*Hybrid - 1 day remote - Fresno*

Opportunities for you!

• Consecutively recognized as a top employer by Forbes
• Vacation time starts building on Day 1, and builds with your seniority
• 403(b) retirement plan with up to 8% matching contributions 
• Free parking and electric charging
• Great food options with on-demand ordering

Commitment to diversity and inclusion is a cornerstone of our culture at Community. All are welcome as valued members of our community.

We know that our ability to provide the highest level of care is through taking care of our incredible teams. Want to learn more? Click here.

Your Career at Community | Opportunity. Challenge. Growth.

We are looking for a Clinical Research Specialist to join our growing team! Working closely with the Principal Investigator, you will be responsible for clinical trials, including facilitating and coordinating daily study activities. In your role, you will consistently have the opportunity to lead our research efforts! You should possess the ability to carry out proper handling of highly sensitive information, all the while following protocol and maintaining IRB approval. From study testing, to enrollment of multicenter clinical trials, to longitudinal cohort studies, your expertise will be essential to the quality improvement of our research process. 

In your role, you will: 

• Participate in the development of accurate source material for training with other clinical departments as required. Prepare and maintain all IRB documentation, including study applications, modifications, renewals, and study closures.
• Provide accurate and timely data collection, documentation, entry and reporting to both sponsor and study specific databases.
• Ensure site compliance with research protocols by reviewing regulatory requirements to confirm implementation of appropriate methods, practices and procedures for all research activities. Ensure compliance with federal, state, and hospital policies and/or procedures. Provide ongoing quality control audits, including maintaining ongoing investigational drug accountability.
• Communicate and collaborate specific study requirements with the PI and other research teams, including internal and external parties, sponsors, monitors, and study participants.
• Monitor patients for study eligibility and assist with the informed consent process from potential research participants. Identify and report issues that may affect the accuracy and quality of the study design.

Licenses and Certifications

• One of the following is required within 1 year of hire or transfer into position
• CRA - Clinical Research Associate
• CCRP - Certified Clinical Research Professional
• BLS - Current Basic Life Support (BLS) for Healthcare Providers by American Heart Association (AHA) required

• Pay ranges listed are an estimate and subject to change.
• If any bonuses are noted, they are only applicable to external hires meeting criteria.