Regulatory Start-Up Specialist 1

    IQVIA Published: November 6, 2020
    Location
    Courbevoie, France
    Job Type

    Description

    The IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. To be part of the Regulatory & Start-Up team will help them to decrease the site activation time and help the site to be ready to recruit patients faster. We seek dynamic and motivated people who truly want to make a difference in the life sciences industry. At IQVIA, we look for the very best people and give them meaningful work to do. We don’t simply think about careers, we think about contributions.

    The RSU specialist will have the following responsibilities :

    • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Leadership. Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines.
    • Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
    • Prepare site regulatory documents, reviewing for completeness and accuracy.
    • Review, prepare and negotiate site contracts and budgets with sites, if applicable.
    • Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
    • Review, track and follow up the progress, the approval and execution of documents, including contracts, regulatory, ethics, ICF and IP Release documents, in line with project timelines.
    • Provide local expertise to RSU leads and Project team during initial and on-going project timelines planning.

    The RSU specialist has :

    • Bachelor’s degree in life sciences or a related field and 1 year’s clinical research or other relevant experience.
    • In-depth knowledge of clinical systems, procedures and corporate standards.
    • Effective communication, organizational, planning, interpersonal skills.
    • Ability to work independently on multiple projects and to effectively prioritize tasks.
    • Knowledge and ability to apply GCP/ICH and applicable regulatory requirements including local regulations, SOPs and company’s corporate standards.
    • Ability to establish and maintain effective working relationships with coworkers, managers and customers.

    The position is located in France, office-based in La Défense, for a 6 months fixed-term contract initially, with potential permanent one.

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