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Clinical Research Coordinator Associate

2+ years
$31.84 – $37.79 per hours
10 April 16, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title:

Clinical Research Coordinator Associate (Hybrid Opportunity)


Job Location:

Stanford School of Medicine, California, USA (Hybrid Eligible)


Company:

Stanford University – Dr. Emmanuel Mignot’s Laboratory, Division of Sleep Medicine, Department of Psychiatry & Behavioral Sciences


Job Type:

Full-time | Regular


Job Code:

1013


Requisition ID:

105868


Posted Date:

February 7, 2025


Role Overview:

The Clinical Research Coordinator Associate will support moderately complex clinical studies within Dr. Emmanuel Mignot’s laboratory, combining clinical and translational research focused on sleep medicine and narcolepsy. This role will serve as the primary point of contact for research participants and stakeholders while ensuring adherence to study protocols and regulatory compliance.


Key Responsibilities:

  • Coordinate clinical studies from start-up to close-out.

  • Determine participant eligibility, obtain informed consent, and assist with recruitment strategies.

  • Manage clinical data, specimens, case report forms, and study documentation.

  • Maintain study budgets and resolve billing issues with finance teams.

  • Prepare regulatory submissions and manage IRB renewals.

  • Act as a liaison for sponsor meetings and regulatory audits.

  • Ensure proper documentation per institutional and regulatory standards.

  • Monitor safety, compliance, and proper conduct throughout the study.


Education & Experience:

  • Two-year college degree + two years of relevant work experience
    OR

  • Bachelor's degree in a related field
    OR

  • Equivalent combination of education and experience

Preferred: Bachelor’s degree + 2 years of clinical trials experience


Skills & Competencies:

  • Strong interpersonal and organizational skills

  • Proficiency in Microsoft Office tools

  • Knowledge of medical terminology

  • Ability to manage multiple tasks with attention to detail


Certifications (Preferred):

  • Certification from SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals)


Physical Requirements:

  • Frequent standing, walking, bending, and fine grasping

  • Occasional sitting, desk work, phone usage, and lifting up to 40 lbs

  • Rare lifting over 40 lbs and physical tasks such as crawling or ladder use


Working Conditions:

  • Occasional evening and weekend work

  • Located at Stanford Redwood City campus (Hybrid)


Compensation:

  • Hourly Pay Range: $31.84 – $37.79

  • Actual pay will be determined by role scope, experience, location, and internal equity