Project Management Officer - Manchester, United Kingdom - Kenton Black Ltd

    Kenton Black Ltd
    Kenton Black Ltd Manchester, United Kingdom

    2 weeks ago

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    Description

    Job Title:
    Analytical Project Manager - GLP

    About Us:

    A Pharmaceutical CRO in the North West is currently seeking a highly skilled and experienced Analytical Project Manager with a strong background in managing projects governed by Good Laboratory Practice (GLP) or Good Clinical Laboratory practice.

    The successful candidate will play a pivotal role in overseeing and coordinating analytical projects, ensuring compliance with GLP guidelines.

    The Analytical Project Manager will collaborate with cross-functional teams, guiding the successful execution of projects while maintaining the highest standards of quality and regulatory compliance.


    Project Planning and Execution:
    Collaborate with internal and external stakeholders to develop project plans and timelines for analytical studies conducted under GLP.
    Ensure the successful execution of projects by coordinating activities, and monitoring progress.

    Stay abreast of GLP regulations, guidelines, and industry best practices to ensure projects are conducted in full compliance with GLP standards.

    Implement and maintain processes for the proper handling, documentation, and reporting of analytical data in adherence to GLP principles.


    Resource Management:
    Allocate resources effectively, including analytical personnel, equipment, and facilities, to meet project timelines and objectives.
    Collaborate with team members to optimize workflows and enhance overall project efficiency.

    Act as a primary point of contact for clients regarding analytical project details, progress updates, and addressing any client-specific requirements.

    Ensure client satisfaction by delivering high-quality analytical data (DMPK / ADME) in accordance with GLP / GCP guidelines.
    Collaborate with the Quality Assurance team to address and resolve any deviations from GLP standards.
    Advanced degree in a relevant scientific discipline (e.g., Industry experience as a scientist generating data for GLP / GCP studies (Bioanalysis / DMPK / ADME)
    Prior industry experience delivering projects in a CRO / Contract testing services on GLP / GCP regulated studies. (Strong understanding of regulatory guidelines, regulatory requirements, and industry standards for analytical studies.
    Excellent project management, communication, and interpersonal skills.