Research Associate III – Clinical Outcomes Assessment

Thermo Fisher Scientific

. Support the Principal Investigator in developing study designs, budgets, and proposals, including outcome selection, sample size, and analysis approach .

Posted 11/12/2026full-timeRemote • Netherlands, Denmark, France, Hungary, Sweden, Italy, Poland, United Kingdom, SpainMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in developing study designs, protocols, and analysis plans while effectively managing qualitative and quantitative data analysis. Proficient in communication and collaboration with stakeholders, ensuring compliance with SOPs and IRB requirements.

Highest-signal resume keywords

PhD In Relevant Scientific DisciplinePatient-Centered Research ExperienceQuantitative Data AnalysisExcellent Communication SkillsMS Word, PowerPoint, And Excel Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Study Design DevelopmentProtocol DevelopmentQuantitative AnalysisQualitative Data AnalysisStatistical Methods FamiliarityTechnical Report WritingBudget ManagementData Quality ControlOutcome Assessment ValidationAnalysis Plan Development

Soft Skills

Analytical SkillsProblem-Solving SkillsDelegation AbilityPrioritization SkillsIndependent Project Management

Tools & Technologies

PubMedLiterature DatabasesElectronic Filing Systems

Industry Keywords

Clinical Outcome AssessmentsPatient Advocacy GroupsIRB ComplianceSOP CompliancePatient-Centered Research

About the role

Key responsibilities & impact

Support the Principal Investigator in developing study designs, budgets, and proposals, including outcome selection, sample size, and analysis approach
Develop protocols, analysis plans, technical reports, and other deliverables for PI and client review
Coordinate and support junior staff throughout projects
Communicate with and manage internal and external stakeholders and vendors, including patient advocacy groups and other departments
Conduct qualitative interview studies and/or surveys with patients, caregivers, and investigators
Contribute to quantitative study approaches, including response options, scoring, and planned analyses
Support development, testing, and validation of fit-for-purpose clinical outcome assessments
Evaluate measurement properties including reliability, validity, responsiveness, and meaningful change
Manage qualitative and quantitative data analysis and quality control, including descriptive and inferential analyses
Review analysis outputs and interpret findings
Contribute to manuscripts, posters, and oral presentations at conferences
Contribute to wider Patient-Centered Research team projects
Track project timelines and budget use with the Project Management Office
Maintain electronic filing, SOP, and IRB compliance
Stay current with relevant research and contribute to PCR initiatives, training, mentoring, team meetings, and organizational discussions
Record project time accurately each week

Requirements

What you’ll need

PhD in relevant scientific discipline, or master’s degree and at least three years of experience in a relevant field, or bachelor’s degree in a relevant scientific discipline and at least five years of experience in a relevant field
Outstanding analytical and problem-solving skills, including ability to assess quantitative data and draw appropriate conclusions
Excellent communication and scientific writing skills
Demonstrated ability to proactively and independently drive research projects
Ability and willingness to delegate and prioritize
Prior experience supporting patient-centered research studies (e.g., COA development and validation studies, ITR)
Proficient in MS Word, PowerPoint, and Excel
Experience in quantitative and/or qualitative data analysis desirable, with quantitative analysis particularly relevant to this role
Familiarity with statistical methods used in patient-centered research, clinical outcomes research, or COA evaluation
Experience with PubMed or similar literature databases advantageous
Ability to complete relevant training courses, follow SOPs and IRB requirements, and communicate effectively with clients