Research Scientist – Patient-Centered Outcomes, In-Trial Research

Thermo Fisher Scientific

. Serve as the independent Principal Investigator for projects .

Posted 10/30/2026full-timeRemote • United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in qualitative research methodologies and project management within the life sciences or social sciences domains. Proven ability to lead scientific projects, manage client relationships, and deliver high-quality outputs while adhering to regulatory standards.

Highest-signal resume keywords

Principal Investigator ExperienceQualitative Research ExpertiseProject Management SkillsClient Relationship ManagementScientific Writing Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Qualitative Research PrinciplesData AnalysisProject DeliveryProposal WritingRegulatory Meeting PreparationBudget ManagementSOP CompliancePatient Experience Data AnalysisMultitaskingScientific Innovation

Soft Skills

LeadershipCommunication SkillsAnalytical SkillsProblem-Solving SkillsCollaboration

Tools & Technologies

Computer-Assisted Qualitative Data Analysis SoftwareAtlas.tiNVivoMAXQDADedoose

Industry Keywords

Clinical TrialsPharmaConsultingClinical Outcome AssessmentFDA Meetings

About the role

Key responsibilities & impact

Serve as the independent Principal Investigator for projects
Oversee all aspects of project delivery and delegate project management tasks to junior scientific staff
Take scientific responsibility for project completion and provide strategic consultation
Use the best methods to address research needs and oversee a large project portfolio
Innovate scientifically and produce high-quality scientific outputs
Conduct qualitative and quantitative scientific work
Present scientific work in peer-reviewed journals and at professional meetings
Provide scientific leadership to team members
Develop and deliver scientific studies and results directly to clients
Advise colleagues on study design and implementation
Contribute to publications, presentations, workshops, advisory boards, and FDA meetings
Develop and maintain client relationships
Advise clients on scientific methods and plans
Help clients prepare for and attend regulatory meetings
Bring in proposal leads, write proposals, manage proposal writing, and close sales
Meet an annual target utilization rate of 60%, unless otherwise specified
Manage internal timelines, project budgets, scope creep, legal and contracting issues
Develop and present internal scientific trainings
Conform to SOPs and Evidera/PPD requirements
Support new product development and scientific innovation

Requirements

What you’ll need

Doctorate in a life sciences or social sciences discipline and more than 3 years’ experience in a relevant field, or Master’s degree in a life sciences or social sciences discipline and more than 5–7 years’ experience in a relevant field
An equivalency consisting of a combination of appropriate education, training and/or directly related experience may be considered sufficient
Experience using Computer-Assisted Qualitative Data Analysis Software (CAQDAS), such as Atlas.ti, NVivo, MAXQDA, or Dedoose
Experience analyzing patient experience data, such as interviews, surveys, and COA (clinical outcome assessment)
Experience managing multiple projects
Deep understanding of qualitative research principles and familiarity with qualitative research in clinical trials
Extensive knowledge of qualitative methods
Advanced understanding of operational and logistical challenges of in-trial research
Well-developed communication and scientific writing skills
Strong analytical and problem-solving skills
Ability to independently manage, oversee, and/or lead project-related tasks and delegate tasks
Ability to manage client relationships
Ability to multitask collaboratively
Experience in pharma or consulting companies preferred
Familiarity working in a clinical research environment preferred

Benefits

Comp & perks

Fully remote work arrangement
Collaboration and development opportunities
Global team environment
Passion, innovation, and commitment to scientific excellence
Opportunities to contribute to scientific publications, presentations, workshops, advisory boards, and FDA meetings
Professional/scientific training and development