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Research Associate, Biomedical Engineering

Advocate Aurora Health
Winston-Salem, United Statesfull_timeVerifiedPosted 12 Aug 2025

About the role

Department:

85082 Wake Forest University Health Sciences - Academic Biomedical Engineering

Status:

Full time

Benefits Eligible:

Yes

Hours Per Week:

40

Schedule Details/Additional Information:

Senior research associate is the position our PhD's typically move to. Typical business hours.

Job Summary:

Functions as expert research associate in coordinating the conduct of system-wide academic and outcomes research. Supports scientists, investigators, and research teams with all phases of research projects, including but not limited to study start-up, data collection, cleaning, and dissemination of findings. Manages and conducts patient screening, enrollment and follow-up associated with prospective observational and/or intervention studies.

Major Responsibilities:

  • Serves as lead research associate in coordinating system-wide academic research activities with scientists and investigators throughout all phases of research projects, including but not limited to study start-up, data collection, cleaning, and dissemination of findings.
  • Plans and implements data collection, management, and cleaning in collaboration with scientists/investigators. Prepares data for preliminary analyses.
  • Independently conducts and coordinates regulatory materials documentation, data collection, and study record maintenance in a timely manner, interfacing with the Institutional Review Board and other offices to facilitate support and reporting of ongoing research.
  • Plans, coordinates and engages clinical staff at sites that are participating in research to encourage patient recruitment and identify creative methods of referring patients.
  • Supports investigators in preparing abstracts, manuscripts, posters, and presentations for publication/presentation; may act as project lead, as well as lead presenter or author, when appropriate.
  • Participates in continuous improvement processes and sharing of best practices across the research offices/departments. Ensures study team is conducting research activities in an ethical and safe manner according to applicable policies, procedures, and regulatory standards.
  • Designs and performs literature searches and results reporting in collaboration with scientists and investigators.
  • Coaches and mentors more junior research associates.
  • May contribute to grant writing and may work with grants team to further manage grant awards.
  • Coordinates project meetings between scientists, teams and collaborators to ensure project success, as needed.

Education Required:

  • Master's Degree.


Experience Required:

  • Typically requires 5 years of experience in Health related and/or research experience (Outcomes Research, Epidemiology, Data Science, Public Health)


Knowledge, Skills & Abilities Required:

  • Ability to successfully coordinate and manage a research study.
  • Experience supporting scientists and investigators in project management and writing research protocols, scientific results or other reports/communications.
  • Excellent verbal and written communication skills; organizational, time management, and multi-tasking abilities to achieve project deadlines. Ability to understand and convey study design and protocol to others through presentations and public speaking.
  • Significant experience in generating and maintaining complex databases and spreadsheets. REDCap experience preferred.
  • Experience in study recruitment activities, including familiarity with regulatory procedures and patient consent processes and requirements.
  • Strong customer service and relationship management skills. Must be able to establish a good rapport with patients, scientists and investigators, clinical team, and external collaborators.
  • Experience in coordinating and facilitating meetings with multiple stakeholders.
  • Proficient in Microsoft applications (Word, Excel, PowerPoint) and related software.
  • Competency in Microsoft applications (Word, Excel, PowerPoint) and Electronic Medical Records (EMR.
  • Experience with IRB submissions and requirements preferred.


Physical Requirements and Working Conditions:

  • Will generally be exposed to rapid-pace an

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Company

Advocate Aurora Health

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