Senior Clinical Research Scientist Jobs in Florida

Job Summary

Responsible for health outcomes research design, data collection and analysis including use of clinical data, questionnaires, and individual/group interviews. Works closely with the research and clinical teams in the planning and conducting of original research, supporting a variety of other research projects and hospital initiatives, preparing reports and scientific publications, and presenting at local and national meetings.

Job Specific Duties

- Conducts studies with clinicians, caregivers, and children at multiple medical centers. Collaborates with study teams and conducts multi-site research.
- Assists study team in developing outcomes measures (e.g., item writing, cognitive interviewing, statistical analysis).
- Prepares presentations and writes scientific publications.
- Creates and maintains data collection forms in RedCap as needed.
- Assists with coding of qualitative data and data entry of questionnaires.
- Manages, cleans, organizes, and conducts analysis of large datasets using a variety of methods.
- Prepares and designs reports, tables, charts, and graphs with written summaries, conclusions, and recommendations.
- Interfaces with internal and external study teams to support best practices in data collection, management, and security.
- Strengthens collaborations with internal and external researchers, with the goal of publishing original articles for the organization.
- Assists with preparing research protocols, consent forms, and other study documents.
- Contributes to identifying potential new funding sources, grant writing, and grant reporting.

Qualifications

Minimum Job Requirements

- Ph.D in Neuroscience
- 4-7 years of work experience in health outcomes or social science measure development and mixed methods research (qualitative and quantitative); (OR) post-doctoral experience.

Knowledge, Skills, and Abilities

- Knowledge of measurement principles, including familiarity with psychometric concepts such as measurement error, validity, reliability, and item response theory
- Experience selecting appropriate methods and conducting statistical analyses with healthcare or social science data sets
- Knowledge of quantitative and qualitative research design, including mixed methods design in the social sciences
- Experience creating or refining survey instruments and other measurement tools
- Demonstrated record of publication (as both first author and collaborator) in peer-reviewed scientific journals and presentations in academic or medical conferences
- Experience with statistical software (SPSS, SAS, or R)
- Experience with, or ability to learn, qualitative analysis software (NVivo or similar)
- Experience creating and managing questionnaires, data collection forms and databases (REDCap or similar)
- Ability to learn new programs and processes easily in a fast-paced environment
- Ability to enter, code, and clean data
- Ability to survey public databases for research purposes
- Experience conducting scientific literature reviews
- Ability to identify and solve a range of problems within area of expertise
- Familiarity with IRB regulatory requirements and processes
- Excellent oral/written communication and interpersonal skills