Clinical Research Associate – Level I or II
Thermo Fisher Scientific
Posted: 10/21/2026Assistant Clinical Research Associate
Thermo Fisher Scientific
Posted: 10/21/2026
Clinical Research Associate
Allucent
Posted: 10/21/2026
Clinical Research Associate I – Clinical Research Associate II
Precision For Medicine
Posted: 10/15/2026
Clinical Research Associate I/II
Precision Medicine Group
Posted: 10/15/2026
Clinical Scientist – Oncology
Excelya
Posted: 10/15/2026
Clinical Research Associate
Novo Nordisk
Posted: 10/14/2026
Clinical Research Associate (CRA) Monitor – Consultant
Ividata Life Sciences
Posted: 10/7/2026
Senior Biostatistician – Biomarker Experience
ICON plc
Posted: 10/6/2026Biostatistician – Biomarker Experience
ICON plc
Posted: 10/6/2026Senior Clinical Research Associate – Contractor
Allucent
Posted: 10/3/2026Clinical Research Associate – Investigator Site
Excelya
Posted: 9/25/2026
Clinical Research Manager – Local Trial Manager
Parexel
Posted: 9/24/2026Clinical Scientist – Immunology
Excelya
Posted: 9/23/2026Senior Clinical Research Associate
Precision For Medicine
Posted: 9/21/2026Senior Clinical Research Associate
Precision For Medicine
Posted: 9/21/2026Senior Clinical Research Associate
Precision For Medicine
Posted: 9/21/2026Senior Clinical Research Associate
Precision For Medicine
Posted: 9/21/2026Senior Clinical Research Associate
Precision Medicine Group
Posted: 9/21/2026Senior Clinical Research Associate
Precision Medicine Group
Posted: 9/21/2026Clinical Research Associate – Level I or II
Thermo Fisher ScientificCore Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical monitoring and site management, ensuring compliance with protocols and regulations while maintaining data accuracy. Proficient in risk-based monitoring and effective communication with investigative sites and clinical teams.
Highest-signal resume keywords
Clinical Monitoring SkillsRisk Based MonitoringICH GCP KnowledgeMedical Terminology UnderstandingBachelor's Degree In Life Sciences
About the role
Key responsibilities & impact- Perform and coordinate clinical monitoring and site management activities
- Conduct remote and on-site visits to assess protocol and regulatory compliance
- Manage clinical trial procedures, guidelines, documentation and audit readiness
- Monitor investigator sites using risk-based monitoring, root cause analysis and corrective/preventive actions
- Ensure data accuracy through source data review, source data verification and CRF review
- Assess investigational product inventory and records
- Document observations and escalate deficiencies through resolution
- Maintain contact with investigative sites between monitoring visits
- Participate in investigator meetings and identify potential investigators
- Initiate clinical trial sites and make recommendations regarding site suitability
- Perform trial close-out and retrieve trial materials
- Ensure essential documents are complete and conduct on-site file reviews
- Provide trial status tracking and progress updates to the Clinical Team Manager
- Update clinical study systems according to study conventions
- Facilitate communication between investigative sites, the client company and the project team
- Respond to company, client and regulatory requirements, audits and inspections
- Complete expense reports and timesheets
- Assist with project publications and tools
- Contribute to project initiatives and process improvement
Requirements
What you’ll need- Bachelor's degree in a life sciences related field, or Registered Nursing certification or equivalent and relevant formal academic/vocational qualification
- Previous experience comparable to 1 year as a clinical research monitor
- Valid driver's license where applicable
- Equivalency of appropriate education, training and/or directly related experience may be considered
- Proven clinical monitoring skills
- Understanding of medical/therapeutic area knowledge and medical terminology
- Working knowledge of ICH GCPs, applicable regulations and procedural documents
- Critical thinking, root cause analysis and problem-solving skills
- Ability to manage Risk Based Monitoring concepts and processes
- Good oral and written communication skills
- Organizational and time management skills
- Effective interpersonal skills and attention to detail
- Ability to work flexibly, adaptably, independently and in a team
- Solid knowledge of Microsoft Office and ability to learn appropriate software
- Fluency in French and good English language and grammar skills
- Good presentation skills
- Ability to travel frequently to site locations
Benefits
Comp & perks- Frequent travel, generally 60-80% but more for some individuals, including possible extended overnight stays
- Work-from-home office environment option
- Personal protective equipment provided/required for applicable exposures
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ManagementSource Data VerificationRoot Cause AnalysisData Accuracy AssessmentTrial Close-Out ProceduresRegulatory ComplianceAudit ReadinessInvestigator Site AssessmentDocumentation ManagementProject Publications Assistance
Soft Skills
Critical ThinkingProblem-SolvingOrganizational SkillsInterpersonal SkillsAttention To Detail
Tools & Technologies
Microsoft OfficeClinical Study Systems
Certifications & Qualifications
Registered Nursing Certification
Industry Keywords
Clinical ResearchLife SciencesMedical/Therapeutic Area KnowledgeRegulatory RequirementsSite Management