Clinical Research Coordinator I (Hybrid) - Orthopedic Surgery

• →Manages time-sensitive study activities within a fast-paced environment, balancing competing priorities across industry-sponsored, federally funded, multicenter, and investigator-initiated studies while maintaining rigorous compliance and operational efficiency.
• →Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
• →Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
• →Ensures timely completion of all protocol requirements (assessment, lab testing, procedures and treatments), to include scheduling and facilitating the patient’s timely completion of protocol requirements; evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
• →Collects clinical data under clinical research protocols.
• →Performs other duties as assigned.

Job Location/Working Conditions:

This role is classified as Hybrid, but requires a strong on-site clinical presence (often 3–4 days/week) to support active patient visits, consenting, and time-sensitive study workflows. Travel between local clinical sites is required and relies on personal transportation.

· On-Site (Clinic/Campus): Participant enrollment, informed consent, specimen handling, and care team coordination across multiple clinic locations.

· Remote (Flexibility): Data entry, administrative tasks, and regulatory prep on non-clinic or low-volume days.

On-site requirements fluctuate dynamically based on clinic volume and recruitment schedules.

• Patient care setting.

• Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).

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