Associate Clinical Research Analyst – Tumor Research

Providence

. Prepare, facilitate, coordinate, and submit documentation required by federal, state, and local regulations and institutional requirements for research .

Posted 11/3/2026full-timeSeattle • Washington • United StatesJuniorMid-Level💰 $31 - $48 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in preparing and submitting regulatory documentation for research, including IRB and FDA submissions, while ensuring compliance with federal, state, and local regulations. Capable of leading and training research assistants to achieve project objectives effectively.

Highest-signal resume keywords

IRB Submission PreparationFDA Submission PreparationRegulatory Compliance KnowledgeResearch Coordination ExperienceHuman Subjects Protection

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory Documentation PreparationInvestigator 1572 FormsInvestigational New Drug ApplicationsDevice SubmissionsEmergency Use SubmissionsHDE SubmissionsSafety ReportsResearch Regulations KnowledgeInstitutional Research RequirementsHealthcare Experience

Soft Skills

LeadershipTrainingPrioritizationWorkflow Scheduling

Industry Keywords

Federal RegulationsState RegulationsLocal RegulationsClinical SettingResearch Compliance

About the role

Key responsibilities & impact

Prepare, facilitate, coordinate, and submit documentation required by federal, state, and local regulations and institutional requirements for research
Prepare IRB submissions to assure the protection of human subjects
Prepare FDA-required submissions, including investigator 1572 forms, investigational new drug applications, device submissions, Emergency Use, HDE, and Safety Reports
Lead Research Assistants on a task basis when applicable
Provide on-the-job training
Set priorities and schedule workflow supporting project objectives

Requirements

What you’ll need

Bachelor's Degree preferably in science, healthcare, pharmacy, or another related field, or significant experience in research coordination or regulatory work may be substituted for educational requirements
2 years of experience in healthcare, research, or a clinical setting
Familiarity with regulatory compliance
Knowledge of federal, state, and local research regulations
Knowledge of institutional research requirements
Ability to prepare IRB submissions protecting human subjects
Ability to prepare FDA-required submissions, including investigator 1572 forms, investigational new drug applications, device submissions, Emergency Use, HDE, and Safety Reports

Benefits

Comp & perks

Retirement 401(k) Savings Plan with employer matching
Medical, dental, and vision health care benefits
Life insurance
Disability insurance
Paid parental leave
Vacation time
Paid holidays
Paid time off for health issues
Voluntary benefits
Well-being resources
Professional growth and career support
Inclusive workplace where diversity is valued