Inspire health. Serve with compassion. Be the difference.
Job Summary
Collaborates with clinicians on literature reviews, research hypothesis, study goals, data collection methods and protocol outline. Develops and authors detailed research protocols and participant consent documents to enable quality data collection. Maintains high level of medical acumen and procedures involved in health / clinical studies. Develops and consults on study documentation to enable protocol compliance and human subject safety. Understands internal data collection tools and procedures. Partners with other research staff to initiate, monitor, and close out studies. Designs and implements research strategies with department researchers. Enhances collaborations between investigators. Performs analysis of ongoing research projects to identify needs. Conceptualizes project ideas with PI's and oversee projects. Functions independently in design under PI lead. Identifies potential funding sources for projects. Serves as a scientific liaison between PI, research team, department administration, and sponsor.
Essential Functions
All team members are expected to be knowledgeable and compliant with Prisma Health's purpose : Inspire health. Serve with compassion. Be the difference.
Collaborates as a member of a research team on the design of research projects. Assists literature reviews, and translation of clinical questions into testable research hypotheses. Participates in the development of operations and procedures for the collection, editing, validation and management of data. Assists in preparing preliminary plan for analysis of a research study; present such plans to the research team and prepare final analysis plans based on team input.
Assists with manuscript edits for projects associated with data collection work in which they are involved. Assists with protocol development and drafting. Assists with grant proposal submissions.
Assists with data management, including submitting data requests to DSC and ITS, manually extracting from EHR records; and cleaning, merging, validating and de-identifying data sets.
Serves as a scientific liaison between Principal Investigators, research team, clinical learners, department administration, research administration, sponsors and DSC / ITS report writers and technical staff.
Assists in creating summaries of research and quality improvement data for social media, website and presentation content.
Perform other duties as assigned.
Supervisory / Management Responsibilities
This is a non-management job that will report to a supervisor, manager, director, or executive.
Minimum Requirements
Education - Doctorate in Biology, Chemistry, Bioanalytical Chemistry, Biomedical sciences, Statistics, Biostatistics, Epidemiology or related field of study.
Experience - No experience defined
In Lieu Of
NA
Required Certifications, Registrations, Licenses
NA
Knowledge, Skills and Abilities
Mathematical skills
Organizational skills
Communication skills
Computer skills (word processing, spreadsheets, database, and data entry)
Working knowledge of Redcap
Knowledge of office equipment (fax / copier)
Ability to complete detailed work accurately.
Work Shift
Day (United States of America)
Location
Greenville Memorial Med Campus
Facility
2237 Emergency Medicine
Department
22371000 Emergency Medicine-Practice Operations
Share your talent with us! Our vision is simple : to transform healthcare for the benefits of the communities we serve. The transformation of healthcare requires talented individuals in every role here at Prisma Health.
Research Scientist • Greenville, SC, United States