Sr. Research Assistant
Core
Manage clinical research projects including participant recruitment, data collection from medical records, informed consent, and outcome evaluation for surgical trials.
Role type
Senior Research Assistant (Clinical Trials)
Builds
Clinical trial data and research manuscripts
Domain
Healthcare / Clinical Research / Orthopedics
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical research methodologies, human subject research ethics, regulatory management, data collection, medical record review, informed consent processes, study database management, statistical methodology basics, professional correspondence
Preferred skills
Clinical Research certification, CITI Training, IRBNet, REDCap, Microsoft Excel, advanced data analysis
Technologies
IRBNet, REDCap, iClinicalTrials.gov
Responsibilities
Serve as main contact for research participants, identify eligible patients, review medical records, conduct informed consent, coordinate follow-up appointments, maintain study records, collect and organize patient data, coordinate with investigators, assist in IRB filings, assist in data tabulation and manuscript writing, participate in smaller clinical studies
Seniority
Senior, hands-on IC with supervisory guidance
