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

🔥 13 hours ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧬 Research Scientist

👻 Ghost score 12%

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• 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 provide strategic consultation • 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 methods and scientific innovation in project plans and study design • Develop and deliver scientific studies and results directly to clients • Support study design and implementation based on subject-matter expertise • Develop and maintain client relationships • Understand pharmaceutical industry and FDA structures • Prepare clients for and attend regulatory meetings • 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, project budgets, staffing hours, scope creep, and legal/contracting issues • Develop and present internal scientific training • Conform to SOPs and Evidera/PPD requirements • Support new product development and scientific innovation

🎯 Requirements

• Doctorate in a life sciences or social sciences discipline and more than 3 years’ experience in a relevant field, or a 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, including interviews, surveys, or clinical outcome assessments (COA) • Experience managing multiple projects • Deep understanding of qualitative research principles and 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 effectively • Ability to manage client relationships • Ability to multitask collaboratively

🏖️ Benefits

• Global team environment • Collaboration and development opportunities • Scientific excellence-focused workplace

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