CRA, Clinician to CRA Program

Thermo Fisher Scientific

. Transition clinician expertise into a Clinical Research Associate role within Thermo Fisher Scientific’s Clinician to CRA Program .

Posted 11/12/2026full-timeRemote • United StatesJuniorMid-Level💰 $80,000 - $133,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical monitoring and site management, ensuring compliance with ICH GCP and regulatory standards while effectively communicating with investigative sites and project teams. Proficient in risk-based monitoring, critical thinking, and problem-solving to enhance clinical trial processes.

Highest-signal resume keywords

Clinical MonitoringICH GCP ComplianceRisk-Based MonitoringCritical ThinkingData Accuracy

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchSource Data ReviewSource Data VerificationCase Report Form ReviewRoot Cause AnalysisTrial Close-OutTherapeutic Area ExpertiseMedical TerminologyRegulatory ComplianceMonitoring Plan Execution

Soft Skills

Communication SkillsInterpersonal SkillsAttention to DetailOrganizational SkillsFlexibility

Tools & Technologies

CTMSMicrosoft Office

Certifications & Qualifications

Clinician Certification

Industry Keywords

Clinical TrialsHematologyOncologyCAR-T TherapyRare DiseaseEndocrinologyNeurologyCardiologyInfectious DiseaseCritical Care

About the role

Key responsibilities & impact

Transition clinician expertise into a Clinical Research Associate role within Thermo Fisher Scientific’s Clinician to CRA Program
Perform and coordinate clinical monitoring and site management activities
Conduct remote and on-site visits to assess protocol and regulatory compliance
Apply risk-based monitoring, root cause analysis, critical thinking, and problem-solving to identify site process failures and corrective/preventive actions
Ensure data accuracy through Source Data Review, Source Data Verification, and Case Report Form review
Assess investigational product inventory and records
Document observations in reports and letters using approved business writing standards
Escalate deficiencies and issues to clinical management and follow them through resolution
Maintain contact with investigative sites between monitoring visits
Conduct monitoring tasks according to the approved monitoring plan
Participate in investigator payments and investigator meetings
Identify potential investigators and initiate clinical trial sites according to procedures
Perform trial close-out and retrieve trial materials
Ensure essential documents are complete and compliant with ICH GCP and regulations
Conduct on-site file reviews
Provide trial status tracking and progress reports
Maintain accurate and current study systems such as CTMS
Facilitate communication among investigative sites, client companies, and internal project teams
Respond to company, client, and regulatory requirements, audits, and inspections
Complete expense reports, timesheets, and other administrative tasks
Assist with project publications/tools and contribute ideas for process improvement
Travel frequently, generally 60–80%, with possible extended overnight stays

Requirements

What you’ll need

Clinicians such as RNs, APRNs, PA’s, MDs, Research Nurse or Clinical Research Coordinator with clinician certification or equivalent and relevant formal academic/vocational training
Comprehensive experience as a clinician in a healthcare environment comparable to at least 2 years
Expertise in a therapeutic area, including Hematology/Oncology, CAR-T and Cell Therapy, Rare Disease, Endocrinology/Diabetes, Ophthalmology, Neurology, Cardiology, Infectious Disease, Respiratory/Pulmonology, Internal Medicine, ICU, or Critical Care, comparable to at least 2 years
Basic medical/therapeutic area knowledge and understanding of medical terminology
Ability to attain and maintain working knowledge of ICH GCPs, applicable regulations, and procedural documents
Good oral and written communication skills
Good interpersonal skills
Customer focus, listening skills, attention to detail, and ability to perceive underlying customer issues
Organizational and time management skills
Flexibility and adaptability
Critical thinking, root cause analysis, and problem-solving skills
Ability to manage Risk Based Monitoring concepts and processes
Ability to work independently or in a team
Solid knowledge of Microsoft Office and ability to learn appropriate software
Good English language and grammar skills
Must comply with specific sponsor/client/site requirements, including possible disclosure of vaccination status or other personal information
Frequent driving to site locations and travel generally 60–80%; role states travel requirement greater than 75%

Benefits

Comp & perks

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and 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 in accordance with company policy
Competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) with the opportunity to purchase company stock at a discount
Global resources, formal training programs, and focused support for career transition
Flexible, regular promotion cycles
Professional development through exposure to therapeutic areas and innovative clinical trials