Clinical Research Coordinator - Asheville - Medasource

    Medasource
    Medasource Asheville

    2 days ago

    Healthcare
    Description

    Position: Clinical Research Coordinator

    Location: Asheville, NC

    Duration: 6 month contract with potential to extend up to 1 year or more

    Pay Rate: starts at $30/hr

    Start Date: ASAP

    Description:

    Responsible for Coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a fundamental understanding of human subject research.

    Duties include but are not limited to:

    · Practice and adhere to the "Code of Conduct" philosophy and "Mission and Value Statement"

    · During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.

    · Performs routine operational activities for multiple research protocols

    · Liaise between site research personnel, industry sponsors, and Supervisor

    · Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable

    · Coordinates schedule of assessments from initial submission of feasibility until study closeout

    · Reviews the study design and inclusion/exclusion criteria with physician and patient

    · Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements

    · Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data

    · Creates study specific tools for source documentation when not provided by sponsor

    · Collects, completes, and enters data into study specific case report forms or electronic data capture systems

    · Generates and tracks drug shipments, device shipments, and supplies as needed

    · Ensures timely and accurate data completion

    · Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations

    · Communicates all protocol-related issues to appropriate study personnel or manager

    · Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required

    · Reviews and responds to any monitoring and auditing findings


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