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  • 1 FTE Global CPM Consultant – ASAP start – Remote working (less than 10% travel) – Global CRO – W2

    My client are a mid-sized CRO who are looking for an Global CPM Consultant. Rates are hourly and open based on Skillset, the range is not the maxium.

    Primary Purpose
    The Global Clinical Project Manager (CPM) is critical to the successful conduct of Biopharmaceutical-sponsored clinical trials as a matrix leader of the core project team. The CPM is responsible for the successful delivery of a Biopharmaceutical project(s) from the development of the RFP including study budget, proposed staffing and timelines. The CPM will be client-facing and serve as the internal lead of the project through the life cycle of the study, ensuring effective project delivery in agreement with contracted project timeline and budget. The CPM directs project delivery by driving team and financial efficiency, work product quality, and is responsible for client satisfaction through strong relationship management.

    Responsibilities

    • Serves as a primary lead in developing RFPs for biopharma clients, identifying appropriate staff, preparing proposal language, and developing budget and timelines in collaboration with leaders and key subject matter experts (SMEs)
    • Ensures that deliverables for the assigned project/s are completed according to the contract budget, schedule, and quality standards. Projects will be effectively managed in all areas of performance
    • Develops successful working relationships with clients, executive management, and project staff and collaborate to manage project issues, proactively identify and mitigate risks and drive milestone achievement
    • Serves as the primary point of contact for biopharma clients and demonstrate proficiency in knowledge and understanding of client needs
    • Tracks project deliverables against contract using tools. Proactively prepare/present study metrics to maintain transparency for internal/external stakeholders. Monitor trends and drive changes to the plan as needed; identify risks to delivery and agree mitigation plans with the project team to be presented to the client
    • Ensures adherence to quality control expectations and milestone timelines for delivery of contractually required reports and deliverables
    • Oversees all project resources (i.e., budget, personnel, and subcontracts)
    • Identifies and manage changes to scope and requests for out-of-scope activities. Collaborate with Business Development, Contracts Department, and executive management to ensure timely execution of contract amendments/change orders. Prospectively manage client expectations
    • Presents in bid defense meetings in collaboration with Business Development
    • Develops study management plans in collaboration with Clinical Study Manager (CSM)/Clinical Team Lead (CTL), Clinical Research Manager (CRA) and other core team members
    • Identifies and documents lessons learned from study successes and challenges to promote
    • Other duties as assigned on a case by case bases

    Experience

    • Bachelor’s degree in a scientific discipline with a minimum 6 years demonstrating scientific principles appropriate in managing a clinical research portfolio inclusive of 4 or more years in a pharmaceutical and/or CRO setting (CRO prefered), serving in a global Clinical Trial Team Lead or CPM role or equivalent position.
    • Demonstrable track-record of success delivering complex/ high priority clinical trials within agreed time, quality and cost working across multiple therapeutic areas, phases 1-4, in a global capacity
    • Demonstrated experience in developing and fostering strong client and internal relationships
    • Thorough understanding of ICH GCP and all applicable global regulatory regulations and guidelines
    • Skilled in MS Office Suite of products and working knowledge of Clinical Trial Management Systems, electronic Trial Master File, and electronic Data Capture systems and solutions
    • Demonstrated experience in managing diverse staff and leading successful teams with direct and indirect supervision responsibilities

    YOU MUST HAVE THE RIGHT TO WORK IN THE USA FOR THIS ROLE

    If this is a role of intrest please share your CV and I will look to reach out as soon as possible, this is a great opportunity and will not be round for long!