Clinical Research Coordinator

Location : Onsite - Merced, CA

Weekly Schedule : Monday - Friday, 8 : 00am - 5 : 00pm

Travel : Yes, 25% of the time

Employment Type : Contract to Hire

Compensation : $36 / hour - $47 / hour. Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and / or other paid time off as provided by applicable law.

Required Education & Experience :

• Bachelors in a science or related field or a combination of education and / or additional job-related experience in lieu of the degree.
• 3 years of experience conducting clinical trials required; worked as primary research coordinator for at least 5 drug or device trials.
• 3 years of experience interacting with patients in a healthcare setting.
• Experience using electronic data capture software and Clinical Trial Management Systems.

Job Summary & Responsibilities :

The Clinical Research Coordinator (CRC) works with the Principal Investigators, co- and sub-investigators, Senior Clinical Research Coordinator, clinical and ancillary departments, IRBs, and industry or government sponsors of research to support the planning, implementation and coordination of clinical trials and other research projects managed by the research institute. Duties may vary depending on the size and complexity of each study.

This role assists with clinical trial or other research project coordination duties as assigned, including but not limited to : research participant recruitment, screening and enrollment; completion of protocol required visits and procedures; collection and reporting of data; coordination of and participation in sponsor monitoring visits or federal audits; query resolution; adverse event reporting, source documentation and research record development and maintenance; study drug accountability; specimen collection, processing and shipment.