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Smyrna

    Quality Assurance GCP - Smyrna, United States - Integrated Resources, Inc

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    Description
    There will be travel
    Preferably Onsite Smyrna 2x week
    Ensure candidates are okay with using their own laptop and downloading *** VDI

    Clinical Development Quality Lead


    Notes from HM:
    Looking for an experienced Clinical Quality Assurance professional to support inspection readiness activities for key clinical program.

    This role will involve working cross-functionally with *** internal departments and external organizations, such as CROs, to resolve quality issues to ensure inspection preparedness.


    Specific responsibilities will include:

    Co-lead inspection preparation meetings with team with a focus on inspection preparation at the study level for a key program.

    Reviewing study related documentation to ensure it is inspection ready.
    Conduct Quality Control checks of the eTMF.
    Support data integrity assessments.
    Support the inspection readiness of investigator sites.
    Conduct inspection risk assessments for CROs and vendors.
    Provide guidance on compliance and regulations and ensure study teams are following targeted SOPs during study.
    Help SMEs in the development of storyboards and functional area presentations.

    The ideal candidate will possess:
    Knowledge and interpretation of GCP regulations and standards, with understanding of phase appropriate application of GCP expectations.
    Direct experience with FDA and/or EMA or other health authority inspections of sponsor, investigator site(s), and/or CRO(s).
    Self-motivated with the ability to take initiative, ownership and manage responsibilities while shifting priorities quickly under tight timelines.

    Strong analytical skills, problem solving techniques, and understanding of ensuring level of effort to address observations/quality issues is commensurate with risk.


    • JOB SUMMARY
    Partnering with internal and external business partners to help with driving quality into the
    clinical development portfolio across the *** sites and departments and provide Clinical
    Development Quality input to cross functional teams dealing with complex and/or important
    projects and issues
    Providing mentoring and guidance to other members of the Clinical Development Quality
    team, supporting the Global Head and/or Regional Heads by deputizing for them at
    meetings on request, and contributing to planning and resource prioritization decisions for
    Clinical Development Quality activities
    Partnering with Development Solutions in driving quality into the clinical activities across
    the *** sites
    Providing quality and compliance oversight as well as investigative support to *** activities regulated by Good Clinical Practices (GCP)


    JOB DESCRIPTION
    sop-af V3.0
    Refer to sop-011813
    Page 2 of 4

    The above description is intended to describe the general content and requirements for the performance of this job. It is
    not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Management has the right to
    assign or reassign duties and responsibilities to this job at any time.
    3. MAJOR ACCOUNTABILITIES
    Describe the main accountabilities for this role including significant tasks, responsibilities and projects
    To lead the development of a risk mitigation program for *** clinical programs,
    prospectively identifying critical quality risk factors and their potential impact, and
    developing efficient processes or solutions to manage the risks
    To lead the overall Inspection Readiness process for preapproval GCP inspections or other
    inspections involving the clinical programs
    To support inspections and investigations conducted by international and national
    authorities, including responsibility for the preparation and hosting of *** sponsor sites for
    inspections
    To independently plan, coordinate and execute Clinical Development Quality activities in
    accordance with the risk mitigation plans to validate the systems and processes
    established to ensure subject safety and protection and to ensure that clinical trials
    performed, and data are generated in compliance with international and national GCPs
    As required, review and coordinate the output of trends from audits and risk analyses
    prepared by colleagues, providing senior management and peers in other departments with
    a summary and analyses of the comparative risks and outcomes across multiple clinical
    programs
    To ensure resolution of audit findings through close collaborations with the audit &
    compliance team. Utilize in-depth knowledge and understanding of current business trends,
    applicable regulations and quality principles, to collaborate effectively and influence
    approaches to quality, and ensure work products and output are aligned with regulatory
    guidelines, ICH-GCP, other applicable regulatory requirements and *** global quality
    standards
    To represent Clinical Development Quality at interdepartmental and project team meetings
    taking the leadership role when required, and dealing with complex and difficult or
    important project issues
    To deliver presentations to peers, senior management, and industry audiences, acting as a
    role model for change
    Helps develop, coach and mentor junior colleagues, generating enthusiasm and
    encouraging new ideas.


    JOB DESCRIPTION

    • EDUCATION
    Education Level
    Describe the minimum level of

    education necessary for this role:
    Bachelors

    Experience
    List the type and length of experience

    10 plus years of background, knowledge and experience
    of the (bio)Pharma industry and applicable technical
    aspects of the business.
    3 to 5 years previous experience on Clinical Quality
    within a CRO or in Pharma

    5. COMPETENCIES
    Include specific skills, behaviors and knowledge necessary to meet the objectives of the role
    In-depth knowledge and understanding of ICH-GCP, applicable regulations (domestic and
    international), quality principles, inspection preparation and hosting, risk management and relevant
    business processes and techniques.


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