Assistant Clinical Research Coordinator
Competitive
You'll complete your application on the employer's website.
Competitive
You'll complete your application on the employer's website.
Job type
Salary
Competitive
Location
Sector
Posted
22 days ago
Avispa is recruiting for a leading university seeking an Assistant Clinical Research Coordinator. The role supports clinical research study coordination and operations, including participant recruitment, data collection, regulatory documentation, and compliance with study protocols and requirements.
Responsibilities
Coordinate study activities by scheduling participant visits, assisting with recruitment, screening, informed consent, follow-up communications, and processing study compensation upon completion
Collect, review, and maintain accurate clinical research data by administering study questionnaires, extracting information from medical records, completing case report forms, and ensuring data quality and completeness
Prepare and maintain regulatory and study documentation, including consent forms, subject logs, correspondence, and other research records in compliance with study protocols and regulatory requirements
Support clinical research procedures by collecting and processing study specimens, performing basic patient measurements and tests (such as vital signs, phlebotomy, and EKG after appropriate training/certification), and preparing specimens for shipment
Maintain study operations by ordering supplies, managing research equipment, collaborating with the study team, and supporting additional study activities as assigned
Preferred
EPIC is preferred
Working toward certification to perform basic patient procedures, such as phlebotomy and EKG
EPIC
Phlebotomy
EKG
Basic patient procedures
Clinical procedure certification
Benefits
Group Medical
Dental
Vision
Life
Retirement Savings Program
PSL
Hybrid: 3-4 days onsite per week
Company
Workforce solutions for technology and healthcare companies
Truckee, California, USA
https://www.avispatechnology.com/
Founded in 2011
51-200 employees
Qualifications
1 year of clinical research or related experience
Experience with clinical research data entry and electronic medical records
General knowledge of medical terminology
Ability to maintain accurate research documentation and regulatory records with strong organizational, communication, and attention-to-detail skills
Valid California Class C Driver's License
EPIC is preferred
Working toward certification to perform basic patient procedures, such as phlebotomy and EKG
1 year of clinical research or related experience.
Required skills
Clinical Research, Clinical Research Data Entry, EPIC, Medical Terminology, Regulatory Documentation, Phlebotomy, Electrocardiography (EKG)
Preferred skills
EPIC is preferred
Experience
1+ years
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