Clinical Services: Clinical Research Associate - Qualitative Methods

We are seeking a motivated and detail-oriented qualitative researcher to join our fast-paced, collaborative environment. The ideal candidate for our Clinical Research Associate - Qualitative Methods position will conduct both qualitative research and prepare high-quality clinical study documentation, including protocols, method validation reports, and scientific publications. 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 successful candidate will have the opportunity to deepen their expertise in qualitative methods and medical writing while generating meaningful insights that support innovation in clinical 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 inform study design as well as support medical device and tool development

Prepare, write, and review clinical study documentation, including protocols, method validation reports, and other regulatory or 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 clinical clients

Stay current with emerging qualitative research methodologies, tools, and industry trends

Core Requirements:

Master’s degree in health or a social science major, or an equivalent combination of education and experience

At least 3 years demonstrated experience in qualitative research methods

2 years of established proficiency with NVivo 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 drug development or medical devices, including the use of Medical Device Development Tools (MDDT), is advantageous.

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 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 $60,000.00-$80,000.00 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.