Clinical Research Associate – Oncology

Thermo Fisher Scientific

Clinical Research Associate monitoring oncology clinical trials for Thermo Fisher Scientific, a life-science technology and services company. Ensuring site compliance, data integrity, documentation, and audit readiness through frequent travel.

Posted 8/6/2026full-time🇻🇳 VietnamJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial monitoring, including risk-based monitoring, data accuracy verification, and compliance with ICH GCPs. Proficient in critical thinking, root cause analysis, and effective communication with investigative sites and project teams.

Highest-signal resume keywords

Clinical Trial MonitoringRisk-Based MonitoringICH GCP KnowledgeRoot Cause AnalysisData Verification

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial Management SystemsMedical TerminologyAnatomy TrainingSource Document ReviewSource Data VerificationTrial Closeout ProceduresObservational ReportingExpense ReportingProject PublicationsProcess Improvements

Soft Skills

Critical ThinkingProblem-SolvingInterpersonal SkillsOrganizational SkillsTime Management

Tools & Technologies

Microsoft OfficeClinical Trial Management Systems

Certifications & Qualifications

Bachelor's Degree in Life SciencesRegistered Nursing Certification

Industry Keywords

Clinical TrialsHealthcareMedical ResearchRegulatory ComplianceInvestigational Product Management

About the role

Key responsibilities & impact

Monitor investigator sites using a risk-based monitoring approach
Apply root cause analysis, critical thinking, and problem-solving to identify site process failures and corrective/preventive actions
Ensure data accuracy through source document review, source data verification, and CRF review
Assess investigational product inventory and records
Document observations in reports and letters and escalate deficiencies to clinical management
Maintain contact with investigative sites between monitoring visits
Conduct monitoring tasks according to the approved monitoring plan
Participate in investigator payment processes and issue resolution
Participate in investigator meetings and help identify qualified investigators
Initiate clinical trial sites according to applicable procedures and regulatory obligations
Perform trial closeout and retrieve trial materials
Ensure essential documents are complete and conduct on-site file reviews
Provide trial status tracking and progress reports
Maintain complete and accurate study systems, including Clinical Trial Management Systems
Facilitate communication among investigative sites, the client company, and internal project teams
Respond to company, client, and regulatory requirements, audits, and inspections
Complete expense reports and timesheets
Assist with project publications, tools, process improvements, and other project initiatives

Requirements

What you’ll need

Bachelor's degree in a life sciences related field, Registered Nursing certification, or equivalent relevant formal academic/vocational qualification
Minimal clinical monitoring experience comparable to 2 years in a clinical environment
Experience in clinical trials, medical terminology, medical research, clinical research, healthcare, or a health sciences field with formal medical terminology and anatomy training
Valid driver's license where applicable
Basic medical and therapeutic area knowledge
Working knowledge of ICH GCPs, applicable regulations, and procedural documents
Good oral and written communication skills
Good interpersonal, organizational, and time management skills
Critical thinking, root cause analysis, and problem-solving abilities
Ability to manage risk-based monitoring concepts and processes
Ability to work independently or as part of a team
Solid knowledge of Microsoft Office and ability to learn appropriate software
Good English language and grammar skills
Willingness to travel frequently, generally 60–80%, including possible overnight stays
Ability to work with potential exposure to biological fluids and infectious organisms
Ability to use required personal protective equipment

Benefits

Comp & perks

Hybrid work arrangement
Home office environment option
Equal opportunity employment
Reasonable accommodation for individuals with disabilities
Personal protective equipment provided/required for work activities