Research Scientist - Patient-Centered Outcomes & In-Trial Research

About the role

Evidera's Patient-Centered Research (PCR) group runs in-trial qualitative research (ITR) studies, combining health sciences, psychometrics, epidemiology, psychology and other social sciences to build clinical outcomes assessments, evaluate patient preferences and utilities, run implementation science studies, Delphi panels and secondary data analyses. The ITR Research Scientist is the independent Principal Investigator of projects, overseeing all aspects of delivery, taking scientific responsibility and advising clients on the best methods.

Key responsibilities

• Lead qualitative (interview) studies and/or surveys in clinical trials, obtaining feedback from patients, caregivers, investigators and study staff on their experience, treatment benefit and burdens of participation
• Apply in-depth knowledge of scientific methods, mainly qualitative but also quantitative, and present work in peer-reviewed journals and at professional meetings
• Provide scientific leadership to team members, advise on methods and design, and deliver high-quality scientific outputs to clients
• Develop client relationships, write proposals, close sales and meet an annual target utilization rate of 60% unless otherwise specified
• Manage internal timelines, budgets and staff hours, scope creep, and legal and contracting issues so that deliverables meet client deadlines
• Help clients prepare for and attend regulatory meetings, and contribute to non-project publications, workshops and advisory boards
• Develop and deliver internal scientific trainings, follow SOPs and support new product development

Required profile

• Doctorate in a life sciences or social sciences discipline (psychology, epidemiology, health services, public health, etc.) with more than 3 years' experience, or Master's degree with more than 5-7 years' experience; equivalency may be considered
• Experience using CAQDAS software (Atlas.ti, NVivo, MAXQDA, Dedoose, etc.) and analyzing patient experience data such as interviews, surveys and clinical outcome assessments
• Experience managing multiple projects; pharma or consulting experience and familiarity with clinical research environments preferred
• Strong communication, scientific writing, analytical and problem-solving skills, and ability to manage client relationships