Clinical Research Assistant Job at SQRL in Walnut Creek
SQRL · Walnut Creek, CA
FULL-TIME
Posted Sep 21, 2026
Job Description
* Great benefits including 401k w/match and 15 days PTO
• Monday-Friday, 8:30 AM - 5 PM
• Great opportunity to get involved in clinical research!
ABOUT OUR CLIENT
Our client is a fast growing site network that currently has over 30 sites and constantly expanding!
They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines.
Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors.
RESPONSIBILITIES
• Assist in coordinating the research trial process with CRCs, Site Managers, and PIs
• Assists in educating patients about the nature of the trials and the benefits and risks of participating
• Determine protocol-related needs to conduct the trial and order supplies and equipment
• Recruits and screens potential patients and obtains informed consent
• Completed source documents and forms to facilitate accurate data collection and record keeping
• Conducts in-service programs and summarizes study schedules to assist in understanding and implementing a protocol
• Schedules patient visits and laboratory and diagnostic test procedures
• Assists with investigational product shipments, storage, and accountability
• Review trends, problems encountered, patient adverse events, and patient progress
• Perform other clinical skills as required by the trial protocol, including vital signs, ECGs and blood glucose testing
QUALIFICATIONS
• 1+ years of experience in a medical setting, working with patients.
• Bachelor's degree preferred
• Phlebotomy and EKG experience preferred
• Familiar with using electronic platforms for medical data
#J-18808-Ljbffr
• Monday-Friday, 8:30 AM - 5 PM
• Great opportunity to get involved in clinical research!
ABOUT OUR CLIENT
Our client is a fast growing site network that currently has over 30 sites and constantly expanding!
They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines.
Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors.
RESPONSIBILITIES
• Assist in coordinating the research trial process with CRCs, Site Managers, and PIs
• Assists in educating patients about the nature of the trials and the benefits and risks of participating
• Determine protocol-related needs to conduct the trial and order supplies and equipment
• Recruits and screens potential patients and obtains informed consent
• Completed source documents and forms to facilitate accurate data collection and record keeping
• Conducts in-service programs and summarizes study schedules to assist in understanding and implementing a protocol
• Schedules patient visits and laboratory and diagnostic test procedures
• Assists with investigational product shipments, storage, and accountability
• Review trends, problems encountered, patient adverse events, and patient progress
• Perform other clinical skills as required by the trial protocol, including vital signs, ECGs and blood glucose testing
QUALIFICATIONS
• 1+ years of experience in a medical setting, working with patients.
• Bachelor's degree preferred
• Phlebotomy and EKG experience preferred
• Familiar with using electronic platforms for medical data
#J-18808-Ljbffr
Benefits
- Paid time off
- Health insurance
Additional Details
- City
- Walnut Creek
- State
- California
- Country
- US
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