RTI International

Senior Researcher-Patient Centered Outcomes Assessment

RTI International$90K — $120K *
US-AnywhereRemote in United States
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Postgraduate master's degree with 8+ years or PhD with 5+ years in patient-centered research.
  • Experience leading complex projects and multidisciplinary teams in a consulting or pharmaceutical setting.
  • Proficient in developing patient-centered evidence-generation strategies for drug development.
  • Demonstrated success in managing client relationships and mentoring junior staff.
  • Proven experience interacting with regulatory agencies like FDA and EMA.
  • Strong record of scientific publications and conference presentations.

Responsibilities

  • Lead patient-centered outcomes research programs from design through delivery.
  • Coordinate multidisciplinary teams to ensure timely and high-quality project completion.
  • Manage project risks, resources, and client expectations effectively.
  • Advise clients on patient-focused drug development strategies.
  • Design and execute qualitative research in collaboration with patients and key opinion leaders.
  • Develop outcome measures and evaluate existing COA programs.
  • Contribute to scientific publications and represent RTI-HS at industry events.

Benefits

  • Opportunity to work on impactful patient-centered research in drug development.
  • Collaborative work environment with multidisciplinary teams.
  • Potential for professional development and mentorship opportunities.
  • Involvement in high-profile projects with pharmaceutical and biotech clients.
  • Access to resources and support for research dissemination.
Full Job Description
RTI Health Solutions is seeking an experienced and highly collaborative Senior Scientist to join our Patient-Centered Outcomes Assessment (PCOA) team. This role is ideal for a senior researcher who thrives at the intersection of hands-on execution, scientific leadership,, and collaboration. As a senior member of the PCOA team, you will lead multidisciplinary project teams while remaining actively engaged in the design, conduct, analysis, interpretation, and dissemination of patient-centered research. You will serve as both a scientific leader and a working manager-providing strategic direction, mentoring staff, and ensuring project success while directly contributing to high-impact client deliverables. You will partner with pharmaceutical and biotechnology clients to generate patient-centered evidence throughout the drug development lifecycle, supporting regulatory, reimbursement, and market access objectives. What You'll Do Key Responsibilities Project and Scientific Leadership • Lead complex patient-centered outcomes research programs from study design through final delivery. • Serve as project lead for multidisciplinary teams, ensuring projects are delivered on time, within scope, and to the highest scientific standards. • Provide strategic oversight of study design, methodology, regulatory engagement, and evidence generation plans. • Manage project risks, client expectations, resource allocation, and team performance. • Serve as a trusted scientific advisor to clients and internal stakeholders. Research Execution and Technical Contribution • Personally contribute to the design, execution, analysis, interpretation, and reporting of qualitative and mixed-methods research studies. • Design and lead qualitative research conducted with patients, caregivers, patient advocates, and clinical key opinion leaders, including both stand-alone and clinical trial-based studies. • Lead the development, adaptation, and evaluation of clinical outcome assessments (COAs), including patient-reported outcomes (PROs), observer-reported outcomes (ObsROs), clinician-reported outcomes (ClinROs), and related measures. • Review and critically appraise published literature, COA development programs, and psychometric evidence. • Develop patient-centered evidence strategies to support regulatory, access & reimbursement, and healthcare decision-making needs. • Contribute directly to study reports, client presentations, evidence dossiers, briefing books, and negotiations with key decision makers to support patient-centered value messaging for medicines. Client Leadership and Business Development • Build and maintain strong relationships with existing and prospective clients. • Lead scientific discussions with pharmaceutical and biotechnology sponsors regarding patient-focused drug development strategies. • Support business development efforts through proposal development, client meetings, capability presentations, and identification of growth opportunities. • Contribute to strategic planning and expansion of RTI-HS PCOA capabilities. Publications, Dissemination, and Thought Leadership • Lead and contribute to scientific publications, conference abstracts, posters, presentations, and manuscripts. • Represent RTI-HS at scientific meetings, industry conferences, and client engagements. • Stay current with evolving regulatory guidance, methodological advancements, and industry best practices in patient-centered outcomes research. People Leadership and Talent Development • Provide day-to-day leadership, mentorship, and coaching to junior and mid-level researchers. • Foster technical excellence, knowledge sharing, and professional development across project teams. • Support staff development through project leadership opportunities, scientific review, and career mentoring. • Contribute to building a collaborative, inclusive, and high-performing team culture. What You'll Need • A postgraduate master's level degree plus a minimum of 8 years of experience conducting patient-centered research, or a PhD plus a minimum of 5 years of experience conducting patient-centered research. • Demonstrated experience leading complex patient-centered research projects and multidisciplinary teams within a consulting, pharmaceutical, regulatory, CRO, or academic research environment supporting patient-focused drug development. • Demonstrated success managing client relationships, mentoring research staff, and leading project teams. • Substantial experience developing and successfully executing patient-centered evidence-generation strategies for pharmaceutical clients. • Proven experience interacting with regulatory agencies, including FDA, EMA, or other global health authorities as well as supporting evidence needs for access stakeholders (payers HTA, and prescribers) . • Experience leading proposal development and contributing to business growth initiatives. • Strong publication record and experience presenting research at scientific conferences. #LI-BM1

About RTI International

RTI International is a nonprofit research organization based in Research Triangle Park, North Carolina. The organization was founded in 1958 as the Research Triangle Institute. RTI International provides research and development services to government agencies, businesses, and other organizations. The organization's areas of expertise include health and pharmaceuticals, education and training, energy and the environment, and social and economic development. RTI International has worked with clients such as the National Institutes of Health, the U.S. Department of Energy, and the World Bank. The organization has offices in the United States and around the world.
Learn more about RTI International
Size
935 employees
Industry
Founded
1958
NASDAQ

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