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Qualitative Research Analyst

Remote:

Full Remote

Experience:

Mid-level (2-5 years)

Work from:

Maryland (USA), United States

Offer summary

Qualifications:

Bachelor’s in a scientific discipline, Minimum 3 years of relevant experience, 1 year working in clinical research, Experience in qualitative and quantitative methods.

Key responsabilities:

Plans and conducts research studies
Records and analyzes data, presents results

Emmes Large http://www.emmes.com

1001 - 5000 Employees

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Job description

Overview

Qualitative Research Analyst - Temporary Part-Time

US Remote

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

The Qualitative Research Analyst participates in the preparation, execution, and reporting for qualitative research trials. The Qualitative Research Analyst works to provide expertise in qualitative and quantitative research methods, data analysis, and dissemination of results in the context of clinical research.

Responsibilities

Plans and conducts research studies.
Records and analyzes data and presents results to senior/other research staff.
Supports interview conduct and analysis by interviewing participants, cleaning and coding interview transcripts, compiling data, and managing necessary tools for these activities.
Records and analyzes data.
Ensures that quality standards are met and coordinates with other research, quality, and/or operations staff.
Performs other duties as assigned.

Qualifications

A bachelor’s in a scientific discipline related to clinical research.
Minimum 3 years’ experience working in psychometrics, or a field relevant to research with human participants.
Minimum of 1 year working in clinical research.
Experience developing study materials for qualitative and quantitative studies, monitoring data collection, analyzing qualitative and quantitative data, and writing up reports of findings.
Competence in qualitative data collection methods, analysis, and reporting (e.g., interview, focus groups, thematic coding).
Competence in quantitative research methods, analysis, and reporting (e.g., clinical trial design, survey administration, interpreting statistical output, creating charts, graphs, tables).
Scientific writing skills.
Strong and clear understanding of responsible conduct of research.
Ability to manage multiple projects simultaneously.
Excellent oral and written communication skills.
Ability to interact with participants and caregivers in a professional and compassionate manner.

Preferred

Familiarity with observational research methods (e.g., video capture).
Experience interviewing study participants.
Familiarity with remote office platforms such as video conference and document sharing.
Proficiency in NVivo qualitative coding software.
Grant writing experience.

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The Emmes Company, LLC is an equal opportunity affirmative action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.