Research Scientist – Patient-Centered Outcomes & In-Trial Research
Thermo Fisher Scientific · BE
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About the Role
Join Evidera's Patient-Centered Research group as a Research Scientist and contribute to innovative, in-trial qualitative research. This role involves overseeing all aspects of project delivery, providing scientific leadership, and developing client relationships within the pharmaceutical industry.
Responsibilities
- Applies in-depth knowledge of scientific methods, mainly qualitative but also quantitative.
- Presents scientific work in peer-reviewed journals and at professional meetings.
- Provides scientific leadership to team members.
- Produces deliverables of high scientific quality.
- Advises and implements best methods and scientific innovation in project plans and design.
- Develops and maintains client relationships.
- Understands pharmaceutical industry/FDA structure.
- Identifies scientific methods/plans that help clients meet their goals.
- Provides scientifically rigorous deliverables that best help clients meet their objectives.
- Helps clients prepare for regulatory meetings and attend regulatory meetings with clients.
- Brings in proposal leads.
- Writes proposals and manages the proposal writing process.
- Closes sales.
- Manages internal timelines to ensure that deliverables meet external client timelines.
- Manages internal budget/staff hours per project not to exceed contracted budget.
- Manages scope creep or out of scope work.
- Manages legal/contracting issues.
- Develops and presents internal scientific trainings.
- Conforms to SOPs and other Evidera/PPD requirements.
- Actively supports new product development and scientific innovation.
Requirements
- Doctorate in a life sciences or social sciences discipline (psychology, epidemiology, health services, public health, etc…) and more than 3 years’ experience in relevant field
- Master’s degree in a life sciences or social sciences discipline (psychology, epidemiology, health services, public health, etc…) and more than 5-7 years’ experience in relevant field
- In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
- Experience using Computer-Assisted Qualitative Data Analysis Software (CAQDAS), such as Atlas.ti, NVivo, MAXQDA, Dedoose, etc. is required
- Experience analyzing patient experience data is required, such as interviews, surveys, COA (clinical outcome assessment).
- Experience managing multiple projects is required.
- Experience in pharma or consulting companies is preferred.
- Familiarity working in a clinical research environment is preferred.
Skills
- Deep understanding of qualitative research principles and familiarity with the conduct of qualitative research in the context of clinical trials
- Extensive knowledge of qualitative methods
- Advanced level understanding of operational and logistical challenges of ITR
- Well-developed communication skills
- Scientific writing skills
- Strong analytical and problem-solving skills
- Ability to independently manage, oversee, and/or lead a variety of project-related tasks and effectively delegates tasks to project team
- Ability to manage client relationships
- Collaborative team member
- Efficient multi-tasking
Location
- North America
- Europe
Work Type
- Office
- Standard (Mon-Fri)
Experience Level
- More than 3 years’ experience in relevant field (with Doctorate)
- More than 5-7 years’ experience in relevant field (with Master’s degree)
Education Level
- Doctorate in a life sciences or social sciences discipline
- Master’s degree in a life sciences or social sciences discipline
About the Company
- When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence.
- You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.