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

Thermo Fisher Scientific

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

Posted 10/28/2026full-timeRemote • North Carolina • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in project management and scientific leadership within the pharmaceutical industry, with a strong focus on qualitative research methods and client relationship management. Capable of delivering high-quality scientific studies and navigating regulatory environments effectively.

Highest-signal resume keywords

Principal Investigator ExperienceProject ManagementQualitative Research MethodsClient Relationship ManagementScientific Writing

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Qualitative Research PrinciplesPatient Experience Data AnalysisComputer-Assisted Qualitative Data Analysis SoftwareProject DeliveryStudy DesignProposal WritingRegulatory Meeting PreparationBudget ManagementTimeline ManagementMultitasking

Soft Skills

Communication SkillsAnalytical SkillsProblem-Solving SkillsLeadershipCollaboration

Tools & Technologies

Atlas.tiNVivoMAXQDADedoose

Industry Keywords

Pharmaceutical IndustryClinical ResearchFDA StructuresSOPsEvidera/PPD Requirements

About the role

Key responsibilities & impact

Serve as the independent Principal Investigator for projects and oversee all aspects of project delivery
Delegate project management tasks to junior scientific staff
Take scientific responsibility for project completion and consult strategically on research needs
Oversee and participate in a large project portfolio
Apply qualitative and quantitative scientific methods
Present scientific work in peer-reviewed journals and at professional meetings
Provide scientific leadership and produce high-quality deliverables
Advise on and implement effective methods and scientific innovation in project plans and study design
Develop and deliver scientific studies and results directly to clients
Assist colleagues with study design and implementation
Develop and maintain client relationships
Understand pharmaceutical industry and FDA structures
Prepare clients for regulatory meetings and attend meetings as requested
Bring in proposal leads, write proposals, manage proposal-writing processes, and close sales
Meet an annual target utilization rate of 60%, unless otherwise specified
Manage internal timelines, budgets, staff hours, scope creep, legal issues, and contracting issues
Develop and present internal scientific training
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
Master’s degree in a life sciences or social sciences discipline and more than 5–7 years’ experience in a relevant field
Equivalency through a combination of appropriate education, training and/or directly related experience may be considered
Experience using Computer-Assisted Qualitative Data Analysis Software (CAQDAS), such as Atlas.ti, NVivo, MAXQDA, or Dedoose, is required
Experience analyzing patient experience data, including interviews, surveys, or clinical outcome assessments, is required
Experience managing multiple projects is required
Experience in pharmaceutical or consulting companies is preferred
Familiarity working in a clinical research environment is preferred
Deep understanding of qualitative research principles 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 effectively
Ability to manage client relationships
Ability to collaborate and multitask

Benefits

Comp & perks

Fully remote work arrangement
Standard Monday–Friday work schedule
Collaboration and professional development opportunities
Scientific training opportunities
Participation in professional meetings, workshops, advisory boards, and FDA meetings
Global team environment
Opportunities to contribute to scientific innovation and new product development