Clinical Research Coordinator RN
Location: San Antonio
Posted on: June 23, 2025
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Job Description:
Screens potential patients for protocol eligibility. Presents
trial concepts and details to the patients, participates in the
informed consent process, and enrolls patients on clinical trials.
Responsible for review of consents to ensure proper execution of
the informed consent process for study subjects. Coordinates
patient care in compliance with protocol requirements. Disburses
investigational drug and provide patient teaching regarding
administration and other patient educational needs. Maintains
investigational drug accountability. Oversees the preparation of
orders by physicians to assure that protocol compliance is
maintained. Working independently, reviews patients for changes in
condition, adverse events, concomitant medication use, protocol
compliance, response to study drug and thoroughly documents and
reports all findings to physician and care team. Enters orders to
assure that protocol compliance is maintained. Communicates with
physician regarding study requirements, need for dose modification,
and adverse event reporting Provide clinical services as required
including patient assessments. Responsible for reviewing protocol
specific billing guides and submitting billing information to
appropriate personnel. Responsible for compiling and reporting
protocol activity, accrual data, and research financials to
practice administration and physicians. May be responsible for the
development of practice research budgets. Maintains regulatory
documents in accordance with USOR SOP and applicable regulations.
Participate in scheduling monitoring and auditing visits. Interacts
with the monitors/auditors while onsite. Provide input in
determining and implementing improvements to policies/processes.
Works with clinic staff to solve complex issues around patient
trial participation. Develops SOPs in collaboration with research
and clinical teams. Due to expertise in subject matter, functions
in a lead role as a resource for research staff. Conduct
protocol-specific training for study personnel to include training
of staff in preparation for study activities Review protocols and
provide input on study activities in relation to areas of
responsibility. May work with SRL to determine study recruitment
and enrollment goals. Oversees subject recruitment and study
enrollment to meet goals. Leads efforts to find effective
strategies for promoting/recruiting research participants and
retaining participants in long-term clinical trials Assists SRL in
feasibility assessments and study selection. Trains and promotes
professional development of staff.
Keywords: , San Marcos , Clinical Research Coordinator RN, Healthcare , San Antonio, Texas
