Clinical Research Associate

2 weeks ago


San Marcos, California, United States GLIA HEALTH MANAGEMENT LLC Full time
Job Overview

Benefits:

  • 401(k) plan
  • 401(k) matching program
  • Competitive salary structure
  • Dental coverage
  • Flexible working hours
  • Health insurance options
  • Career advancement opportunities
  • Paid time off policies
  • Training and development programs
  • Vision coverage
  • Wellness resources available

GLIA HEALTH MANAGEMENT LLC is a dynamic outpatient neurology practice dedicated to providing exceptional patient care. We are looking for a healthcare professional who is committed to delivering quality care and positively impacting our patients' lives. Join our talented research team and be part of our ongoing clinical trials.


The ideal candidate is a pre-med student, foreign medical graduate, or medical assistant with a genuine curiosity and passion for healthcare.


Why Become Part of Our Team?

  • Attractive compensation package
  • Comprehensive health insurance coverage: Medical and Dental
  • Retirement savings plan with dollar-for-dollar matching
  • Accrued paid vacation time
  • Paid holidays
  • Paid training sessions
  • Collaborate with highly skilled and specialized physicians
  • Promote a healthy work-life balance

Position Summary
The Clinical Research Associate will assist investigators in coordinating clinical trial recruitment, participant screening, and visit intake processes.


Key Responsibilities:

  1. Coordinate participant recruitment for clinical trials, ensuring adherence to the protocol schedule and accurate data entry.
  2. Assist in recruiting participants using regulatory-approved documents and procedures; schedule pre-screening and screening activities, and maintain a current list of potential participants in compliance with applicable regulations.
  3. Monitor participant progress throughout the study, manage participant study binders, and ensure that principal investigators complete their tasks for each visit.

Preferred Qualifications:

  1. Experience as a Clinical Research Coordinator or Research Assistant (CRC/CCRC)
  2. Familiarity with venipuncture techniques
  3. Associate's or Bachelor's degree in a relevant field preferred
  4. Experience with Electronic Health Record systems preferred
  5. Understanding of clinical research policies and guidelines from regulatory bodies such as:
  • U.S. Food and Drug Administration (FDA)
  • National Institutes of Health (NIH)
  • Human Research Protection Program (HRPP)
  • International Council for Harmonization Good Clinical Practice (ICH/GCP)

Employment Conditions:

  1. Proof of COVID-19 vaccination is required.

Knowledge, Skills, and Abilities:

  1. Self-motivated with a strong desire to learn and grow within the healthcare field
  2. Exceptional attention to detail
  3. Strong analytical and critical thinking abilities
  4. Excellent verbal and written communication skills, with the ability to effectively engage with patients, providers, and payors
  5. Ability to prioritize and manage multiple tasks efficiently
  6. Commitment to fostering an ethical work environment
  7. Proficient in computer-based systems such as Excel, Word, and the Internet, with a capacity to quickly learn new technologies
  8. Bilingual in English and Spanish is preferred

Work Schedule:

  • 8-hour shifts
  • Monday to Friday


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