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

Thermo Fisher Scientific

. Serve as the independent Principal Investigator of projects and oversee all aspects of project delivery .

Posted 10/30/2026full-timeRemote • United Kingdom, France, Serbia, Netherlands, Portugal, Italy, BelgiumMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in qualitative research methods and project management within the life sciences or social sciences, with a strong focus on client relationship management and scientific deliverables. Proven ability to lead projects, mentor junior staff, and navigate regulatory environments effectively.

Highest-signal resume keywords

Doctorate In Life Sciences Or Social SciencesExperience Using CAQDASExperience Analyzing Patient Experience DataStrong Analytical And Problem-Solving SkillsExperience Managing Multiple Projects

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Qualitative Research PrinciplesQualitative MethodsProject ManagementScientific WritingClient Relationship ManagementProposal WritingStudy DesignData AnalysisRegulatory Meeting PreparationBudget Management

Soft Skills

Communication SkillsLeadershipCollaborationMultitaskingDelegation

Tools & Technologies

Atlas.tiNVivoMAXQDADedoose

Industry Keywords

Clinical ResearchPharmaConsultingSOPsEvideraPPDClinical Outcome Assessment

About the role

Key responsibilities & impact

Serve as the independent Principal Investigator of projects and oversee all aspects of project delivery
Delegate project management tasks to more junior scientific staff
Take scientific responsibility for project completion and provide strategic consultation
Apply in-depth scientific methods, mainly qualitative and also quantitative
Present scientific work in peer-reviewed journals and at professional meetings
Provide scientific leadership and produce high-quality scientific deliverables
Advise on and implement methods and scientific innovation in project plans and design
Develop and deliver scientific studies and results directly to clients
Assist colleagues with study design and implementation
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 annual target utilization rate of 60%, unless otherwise specified
Manage internal timelines, budgets, staff hours, 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 relevant field
Master’s degree in a life sciences or social sciences discipline and more than 5-7 years’ experience in 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, Dedoose, etc. is required
Experience analyzing patient experience data, such as interviews, surveys, and COA (clinical outcome assessment), is required
Experience managing multiple projects is required
Experience in pharma or consulting companies is preferred
Familiarity working in a clinical research environment is preferred
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 effectively delegate tasks
Ability to manage client relationships
Ability to collaborate and efficiently multitask

Benefits

Comp & perks

Global team environment
Collaboration and development opportunities
Opportunity to contribute to scientific excellence and breakthroughs