Research Associate - Neurosciences - FT
advocate aurora healthCharlotte, NC
Research Associate - Neurosciences - FT
Occupations
Clinical Research CoordinatorsSocial Science Research AssistantsLife, Physical, and Social Science Technicians, All OtherIndustries
Research and Development in the Physical, Engineering, and Life SciencesResearch and Development in the Social Sciences and HumanitiesResearch and Development in BiotechnologyAbout the role
Major Responsibilities Serves as a supporting research associate on department studies across multiple sites. Manages timelines and deliverables. Supports investigator-initiated trials with REDCap project build and ongoing support Performs data abstraction and reporting for a large longitudinal study Ensures appropriate completion and documentation of regulatory materials, source documentation, data collection, and study records in a timely manner. Ensures study team is conducting research activities in an ethical and safe manner according to applicable policies, procedures, and regulatory standards. Serves as a resource to the manager, other research team members, investigators and collaborators, related to particular projects, research procedures, and policies. Supports investigators in preparing abstracts, manuscripts, posters, and presentations Interface with the Institutional Review Board and other AARI and AAH offices/departments to facilitate support and reporting of ongoing research. Coordinates project meetings between investigators, teams and collaborators to ensure project success. Licensure, Registration, and/or Certification Required None Required. Education Required Bachelor's Degree in Health Science or related field.
Experience Required:
Typically requires 2 years of experience in Health related and/or research (Outcomes Research, Epidemiology, Data Science, Public health)
Knowledge, Skills & Abilities:
Required Ability to understand and communicate research protocol requirements to others. Some experience writing standard operating procedures (SOP), experimental protocols, scientific results or similar. Good verbal and written communication skills. Good organizational and time management skills with the ability to work under pressure, meet deadlines and work with a high degree of accuracy. Some experience with developing and maintaining a variety of databases and spreadsheets, generating a variety of reports and dashboards. Ability to problem solve and work independently with a high degree of accuracy and attention to detail. Proficient with Microsoft (Word, Excel, PowerPoint) and related software. Must be able to establish a good rapport with patients, investigators, clinical team, and external collaborators. Competency in using Electronic Medical Record (EMR). Experience in Epic is a plus.
Physical Requirements and Working Conditions:
Will generally be exposed to rapid-pace and complex health care environment.
Remote work with in-person presence (e.g., site visits, recruitment activities, meetings) as needed.
This position may require ability to drive and/or travel to work related meetings/functions and thus is exposed to road, weather, and normal travel hazards.
This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the incumbent. Incumbent may be required to perform other related duties.
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JOB OVERVIEW
Experience level
Mid
Location
Charlotte, NC
Occupation
Clinical Research Coordinators
Industry
Research and Development in the Physical, Engineering, and Life Sciences
Posted
today
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