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We are seeking a motivated and detail-oriented Qualitative Clinical Outcomes Researcher, with strong medical writing skills to join our fast-paced, collective team focusing on the design, conduct, and analysis of qualitative studies (e.g., patient and clinician interviews, thematic analysis, cognitive debriefing) and the preparation of regulatory and scientific documentation. The right candidate will excel in collaboration while working independently as well, has strong communication and organizational skills with the ability to multi-task and prioritize, and is driven to deliver high-quality, evidence-based insights that shape clinical research outcomes. The ideal candidate will have a passion for translating qualitative findings into meaningful clinical insights through collaboration with a multidisciplinary team and engagement in medical writing that drives innovation in clinical science, with the opportunity to further develop their expertise and grow within an expanding team. This position is non-laboratory and ideal for candidates experienced in qualitative health research, patient-reported outcomes, or clinical communication rather than bench science.
Job Responsibility:
Develop and implement qualitative research protocols
Conduct concept elicitation and cognitive debriefing interviews
Perform coding and thematic analysis of qualitative data
Carry out literature reviews to support study design, outcome development, and clinical, commercial or regulatory activities
Prepare, write, and review study documentation, including protocols, qualitative study reports, and study-related materials, ensuring compliance with applicable standards
Contribute to the preparation of scientific manuscripts and publications
Interpret and summarize findings in clear, actionable formats for study sponsors
Stay current with emerging qualitative research methodologies, and industry trends
Requirements:
Master’s degree in public health, psychology, health communications or a social science major, or an equivalent combination of education and professional experience
2+ years’ experience conducting qualitative research in a clinical, health outcomes, regulatory or academic setting
Demonstrated proficiency with NVivo or equivalent qualitative analysis software
Experience conducting systematic literature review(s) and in medical writing such as protocols, reports, or scientific publications
Ability to clearly convey complex findings to audiences of varying expertise, detail oriented, and strong critical thinking/problem solving skills
Proficiency utilizing Microsoft office suite
Nice to have:
Experience in the development of patient and clinician reported outcomes
Familiarity with regulatory processes for clinical studies or medical devices
What we offer:
Paid days off
Medical, dental, and vision insurance
May be eligible for a discretionary bonus
401(k) plan with employer match (currently set at 50%)
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