Senior Clinical Research Associate

Thermo Fisher Scientific

. Perform and coordinate all aspects of clinical monitoring and site management for a dedicated client .

Posted 11/5/2026full-timeRemote • Colorado • United StatesSenior💰 $90,000 - $113,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical monitoring and site management, with a strong focus on data accuracy, regulatory compliance, and effective communication with investigative sites and clients. Proficient in applying critical thinking and problem-solving skills to enhance trial processes and outcomes.

Highest-signal resume keywords

Clinical Trials MonitoringICH-GCP GuidelinesCTMS ExperienceCritical ThinkingOncology Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data AccuracyRoot Cause AnalysisProblem-SolvingSite ManagementTrial CloseoutMonitoring Plan ExecutionPhysical Inventory AssessmentReport DocumentationProcess ImprovementRegulatory Compliance

Soft Skills

Strong CommunicationCollaboration SkillsOrganizational SkillsAttention to DetailGood Judgement

Tools & Technologies

CTMSTrial Management Platforms

Certifications & Qualifications

Bachelor's Degree in Life SciencesRegistered Nursing Certification

Industry Keywords

OncologyClinical MonitoringInvestigational ProductRisk-Based MonitoringSOPs

About the role

Key responsibilities & impact

Perform and coordinate all aspects of clinical monitoring and site management for a dedicated client
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 SDR, SDV, and CRF review during on-site and remote monitoring
Assess investigational product through physical inventory and records review
Document observations in reports and letters using approved business writing standards
Escalate deficiencies and issues to clinical management and follow them through resolution
Maintain regular contact with investigative sites between monitoring visits
Conduct monitoring tasks according to the approved monitoring plan
Participate in investigator payments and investigator meetings
Track trial status and provide progress updates to the Clinical Trial Manager
Update study systems, including CTMS, and perform required CTMS report quality checks
Identify potential investigators and initiate clinical trial sites
Ensure trial closeout, retrieval of materials, and completion of essential documents
Conduct on-site file reviews
Contribute to project publications, tools, process improvements, and other assigned study tasks
Facilitate communication among investigative sites, the client company, and project team
Respond to company, client, and regulatory requirements, audits, and inspections
Complete administrative tasks such as expense reports and timesheets

Requirements

What you’ll need

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification
3+ years of comparable experience
Oncology experience preferred
Strong critical thinking and problem-solving skills
Excellent remote and on-site clinical trials monitoring skills
Understanding of ICH-GCP guidelines, applicable regulations and SOPs
Ability to evaluate data and resolve diverse problems
Good judgement in selecting methods and techniques for solutions
Strong communication and collaboration skills
Ability to interact effectively with investigative sites, clients, and internal teams
Ability to represent the client while maintaining professional relationships
Advanced written and oral communication skills
Strong organizational skills and attention to detail
Experience with computer systems including CTMS and other trial management platforms
Ability to travel >75% for site monitoring activities

Benefits

Comp & perks

Variable annual bonus based on company, team, and/or individual performance results
Choice of national medical and dental plans
National vision plan, including health incentive programs
Employee assistance and family support programs
Commuter benefits
Tuition reimbursement
At least 120 hours paid time off (PTO)
10 paid holidays annually
Paid parental leave: 3 weeks for bonding and 8 weeks for caregiver leave
Accident and life insurance
Short- and long-term disability
401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) with opportunity to purchase company stock at a discount