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Clinical Research Coordinator

Job

Nor Cal Clinical Research

Rocklin, CA (In Person)

Full-Time

Posted 1 week ago (Updated 1 week ago) • Actively hiring

Expires 6/28/2026

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Job Description

Clinical Research Coordinator Nor Cal Clinical Research - 5.0 Rocklin, CA Job Details Full-time $20 - $30 an hour 22 hours ago Benefits Paid holidays Health insurance Dental insurance 401(k) Paid time off Vision insurance 401(k) matching Qualifications Laboratory procedures Data collection Research participation FDA regulations Full Job Description Nor Cal Clinical Research is seeking a motivated individual to conduct and support clinical research focused on holistic and integrative therapies as well as pharmaceutical interventions. Our research program is expanding, and we are seeking additional clinical research coordinators to join our reputable research team. The CRC will be responsible for coordinating clinical research studies. They will be responsible for studies from start up to close out. This candidate will work closely with Principal Investigator (PI) and Sub-investigators as well as other CRCs, Research Fellows and research assistants. Specific duties will include recruiting and screening study subjects and overseeing study visit procedures in accordance with FDA Regulations and Good Clinical Practices. ISSR operates Monday through Friday | 8:30am - 5:00pm In this role you will be expected to perform the following duties:
  • Organize and run clinical studies
  • Actively recruit participants. Calling and following up with potential research patients to inform them about research studies and assess patient interest
  • Manage of and perform clinical study procedures such as blood draws, maintenance of regulatory binders up to date, update data collection databases and answer queries in a timely fashion
  • Perform laboratory processing as needed for study protocols and organize shipments of labs in a timely fashion
  • Maintaining accurate and complete study records by FDA regulations as well as sponsor/CRO and IRB regulations and guidance, study records
  • Communicate with study monitors and organize responses and queries to monitoring visit reviews
  • Proactively focus on clinical trial organization
  • Keep invoices up to date for studies and to make sure you have the unit ready for internal and external audits
  • Assist with other needs in the clinical trials unit as they arise and/or as directed by your supervisors
  • Other duties as assigned or directed by the site manager and director
Preferred:
  • Phlebotomy training and experience with pediatric blood drawing
  • Must be able to occasionally work hours other than Monday through Friday 8:00 a.
m. to 5:00 p.m. due to operational needs. Must be willing to work a flexible schedule as necessary to meet deadlines.
Job Type:
Full Time Salary:
$20 per hour -$30 per hour depending on experience.
Benefits:
  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • Bonus, PTO, Paid Holidays
  • 401k
Match Physical Setting:
Clinic Work Location:
Sacramento Job Type:
Full-time Pay:
$20.00 - $30.00 per hour
Benefits:
401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance
Work Location:
In person