Job opportunity
Clinical Research Assistant Richmond
Headlands Research, Inc.
Support clinical trial visits and participant screening as a Clinical Research Assistant at Richmond Clinical Trials in Richmond, BC. Work onsite Monday through Friday.
Headlands Research seeks a Clinical Research Assistant for its Richmond Clinical Trials site. You will support Clinical Research Coordinators, Investigators, and cross-functional teams during trial execution. The work includes vital signs, phone calls, electronic data entry, and study documentation.
Key Responsibilities:
Assist coordinators with protocol-compliant clinical trial visits
Collect and record participant vital signs
Make study-related phone calls and document electronic data
Support subject screening, enrollment, and follow-up
Verify study documentation accuracy and completeness
Requirements:
Medical terminology and basic laboratory procedures familiarity preferred
Direct hands-on patient care experience preferred
Clinical research experience preferred
Strong attention to detail and time management
Excellent interpersonal skills with participants, providers, and sponsors
Apply clinical experience, participant communication, and accurate data documentation to support regulated clinical trials onsite in Richmond, BC.
#J-18808-Ljbffr
Apply on source site Headlands Research seeks a Clinical Research Assistant for its Richmond Clinical Trials site. You will support Clinical Research Coordinators, Investigators, and cross-functional teams during trial execution. The work includes vital signs, phone calls, electronic data entry, and study documentation.
Key Responsibilities:
Assist coordinators with protocol-compliant clinical trial visits
Collect and record participant vital signs
Make study-related phone calls and document electronic data
Support subject screening, enrollment, and follow-up
Verify study documentation accuracy and completeness
Requirements:
Medical terminology and basic laboratory procedures familiarity preferred
Direct hands-on patient care experience preferred
Clinical research experience preferred
Strong attention to detail and time management
Excellent interpersonal skills with participants, providers, and sponsors
Apply clinical experience, participant communication, and accurate data documentation to support regulated clinical trials onsite in Richmond, BC.
#J-18808-Ljbffr