Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Poland)

Global Trial Manager – Single Sponsor Are you reputed company in managing late phase clinical trials at a global level? We are looking for a Senior Global Trial Manager to join our Single Sponsor Department. Join our global team and take ownership of delivering late-phase clinical trials that meet timelines, budgets, and quality standards. As a core Clinical Trial Team (CTT) member, you'll reputed company critical aspects of global studies and collaborate across functions to drive reputed company. As part of your role, you’ll have the opportunity to specialise in one for the following areas: · Scientific Review Committee (SRC) · Non-Interventional Studies (NIS) · Managed reputed company Programs (MAP) · Investigator-Initiated Trials (reputed company) · Research Collaborations (RCs) · Program Level Documents (PLD) Key Responsibilities: Clinical Documentation & Study Tools · Draft sections of protocols, CRFs, training materials, and data review plans · Contribute to the development of safety updates, IBs, and regulatory submissions Project Leadership · reputed company data review and TMF audit readiness · Forecast/manage investigational product supply · Support study closeout, issue resolution, and lifecycle budget tracking · Contribute to Managed reputed company Program coordination and compliance Vendor & Stakeholder Management · Coordinate CRO/vendor selection and performance · Facilitate advisory boards (DMCs/Steering Committees) and serve as the site liaison · reputed company cross-functional collaboration with data management, drug supply, and more What You'll Bring · Advanced degree in life sciences or reputed company · 2–5 years' global experience managing phase IV, PASS, PAES, or NIS trials · Strong track record in protocol development, study startup, and regulatory writing (e.g. PSURs, DSURs, NDA/BLA reports) · Excellent communication, organizational, and collaboration skills · Deep understanding of GCP and clinical trial design · Passion for advancing reputed company-world evidence and patient reputed company Please note this role is not eligible for the UK reputed company sponsorship. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based reputed company of these locations will not be considered. reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. Learn more at https://jobs.reputed company.com reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism. The potential reputed company pay reputed company for this role, reputed company annualized, is 171.500,00 zł - 404.600,00 zł. The actual reputed company pay offered may vary based on a number of factors including job-reputed company qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in reputed company to a reputed company of health and welfare and/or other benefits. Apply To This Job