Job Description

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 Description:

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

Core 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

Desired Requirements:

Experience in the development of patient and clinician reported outcomes

Familiarity with regulatory processes for clinical studies or medical devices

Canfield Scientific, Inc. is a core imaging lab providing custom photographic systems, image monitoring, and centralized analysis services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and supporting documentation. Canfield offers comprehensive benefits to its eligible full-time employees. These include paid days off, medical, dental, and vision insurance, may be eligible for a discretionary bonus, and a 401(k) plan with employer match (currently set at 50%). The anticipated salary range for the position is $65,000.00-$85,000.00 annually. This is dependent upon consideration of multiple factors when determining a base salary such as a candidate’s experience, education, and current market conditions. If the role is eligible for full benefits, it will be discussed with you during the interview process. Canfield's imaging equipment leads the industry providing high-quality, registered, reproducible clinical images. This, together with proactive clinical image monitoring and a world class quality assurance regimen, sets the gold standard in image quality for clinical studies.

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