Trabajos

    Sr CRA - Buenos Aires, Argentina - Thermo Fisher Scientific

    Thermo Fisher Scientific
    Thermo Fisher Scientific Buenos Aires, Argentina

    hace 6 horas

    Thermo Fisher Scientific background
    De jornada completa
    Descripción
    Job Description

    Monitors investigator sites with a risk-based monitoring approach, applies root
    cause analysis (RCA), critical thinking and problem-solving skills to identify site
    processes failure and corrective/preventive actions to bring the site into
    compliance and decrease risks. Ensures data accuracy through SDR, SDV and
    CRF review as applicable through on-site and remote monitoring activities.
    Assess investigational product through physical inventory and records review.
    Documents observations in reports and letters in a timely manner using
    approved business writing standards. Escalates observed deficiencies and issues
    to clinical management expeditiously and follow all issues through to resolution.
    May need to maintain regular contact between monitoring visits with
    investigative sites to confirm that the protocol is being followed, that previously
    identified issues are being resolved and that the data is being recorded in a
    timely manner. Conducts monitoring tasks in accordance with the approved
    monitoring plan. Participates in the investigator payment process. Ensures a
    shared responsibility with other project team members on issues/findings
    resolution. Investigates and follows-up on findings as pplicable

    • Provides updates on potential trends noted across multiple sites and discusses
    potential strategies for their management to the Clinical Team Manager (CTM).

    • Participates in investigator meetings as necessary. Identifies potential
    investigators in collaboration with the client company to ensure the acceptability
    of qualified investigative sites. Initiates clinical trial sites according to the
    relevant procedures to ensure compliance with the protocol and regulatory and
    ICH GCP obligations, making recommendations where warranted. Ensures trial
    close out and retrieval of trial materials.

    • Ensures that required essential documents are complete and in place, according
    to ICH-GCP and applicable regulations. Conducts on-site file reviews as per
    project specifications.

    • Contributes to the project team by mentoring new members, assisting in
    preparation of project publications/tools including informed consents, CRF
    guidelines and monitoring plans, and sharing ideas/suggestions with team
    members. Assists in project specific training for the clinical team where
    necessary. Identifies areas for potential process improvements & share potential
    solutions for improvements.

    • Performs additional tasks as assigned by CTM or Clinical Manager of CRAs (CMCRA) (e.g. trip report review, newsletter creation, lead CRA team calls etc).
    • Provides trial status tracking and progress update reports to the Clinical Team
    Manager (CTM) as required. Ensures study systems are updated per agreed
    study conventions (e.g. Clinical Trial Management System, CTMS). Perform QC
    check of reports generated from CTMS system where required.

    • Facilitates effective communication between investigative sites, the client
    company and the PPD project team through written, oral and/or electronic
    contacts.

    • Responds to company, client and applicable regulatory
    requirements/audits/inspections federal regulatory requirements/audits.

    • Maintains & completes administrative tasks such as expense reports and
    timesheets in a timely manner

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