| Job Description: |
• Assist with coordination and implementation of clinical research studies within Dr. Ronald Staud’s laboratory.
• Assist with participant screening, recruitment, enrollment, scheduling, and follow up activities.
• Support informed consent activities in accordance with approved study protocols and institutional requirements.
• Coordinate and support research visits, study procedures, and collection of research data and specimens.
• Maintain accurate and complete study documentation, source records, case report forms, and electronic databases.
• Enter research data and assist with responding to data queries and maintaining data quality.
• Assist with IRB submissions, amendments, continuing reviews, regulatory documentation, and maintenance of essential study files.
• Follow approved research protocols, institutional policies, Good Clinical Practice requirements, and applicable regulatory requirements.
• Work closely with the current Clinical Research Coordinator to learn established study workflows, protocols, systems, and laboratory procedures.
• Participate in structured cross training and knowledge transfer to develop competency in critical research responsibilities and ensure continuity of study operations.
• Provide research coordination coverage and operational support as competency is established.
• Assist with study monitoring, audits, study initiation, closeout, and other research activities as assigned.
• Communicate effectively with the Principal Investigator, research staff, clinical personnel, study participants, and other research partners.
• Perform other duties related to clinical research activities as assigned.
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