FSP RA - Client Dedicated - CMC Project Manager

Thermo Fisher ScientificRemote, BelgiumremoteSalary not postedView the original posting at Thermo Fisher Scientific ↗

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Regulatory Affairs Manager – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. To further strengthen our Project Management team, we are looking for a talented CMC Project Manager. This position will occupy a key role supporting Chemistry, Manufacturing and Controls (CMC) development for our therapeutic antibodies, ensuring that projects successfully move forward within and across functions. You will perform planning, controlling, monitoring and reporting for assigned project in collaboration with the CMC Leads and the project teams. This includes CMC activities like process development, analytical development, product development, technical transfer, dossier development, clinical manufacturing and project strategy. The ideal candidate will be detail driven and have a proven track record driving project success within CMC in the pharma/biotech industry. As part of our global team, you’ll have the opportunity to provide technical and project leadership over a client Project. As a Regulatory Affairs Manager, you'll offer innovative solutions, including regulatory affairs expertise and client interface, to provide strategic regulatory intelligence and guidance supporting product development from preclinical stages through registration and product optimization. You will provide strategic, expedient, and efficient preparation of client deliverables that meet current local, regional, and ICH regulatory and technical requirements. Additionally, you will act as a liaison with internal and external clients in the provision and marketing of these services. What You’ll Do: Responsible for achieving project goals, including timelines, budget, and scope. Translate the scientific strategy into a CMC project plan with support of the CMC leads for one or more drug development programs/projects, visualising timelines and dependencies between deliverables and define budget needs Track, monitor and report key milestones and decision points to drive delivery of projects in accordance with corporate objectives., balancing scope, cost, timelines and risk; Build strong working relationships with internal and external key stakeholders to ensure timely completion of CMC activities by continuously monitoring progress; Perform critical path analysis and risks, taking into account cross-functional interdependencies in the overall development project plan; Coordinate on the delivery of those critical path items through prioritization setting where required and mitigate or escalate the risk together with the project team; Perform scenario simulations and advise on optimum development planning, as needed; Prepares and leads project team meetings including issuance of agenda, actions and meeting minutes to be documented, communicated and committed. Promote a culture of collaboration, cooperation, execution excellence, effective communication, and cross-functional problem-solving to enable a high-performing team. • Provides senior review and advice to prepare regional regulatory submissions and ensure high quality standards that meet or exceed client expectations, local and regional requirements. • Acts as subject matter expert in providing regulatory strategy advice and technical expertise to internal and external clients and for key client projects ofmoderate to high complexity. Provides internal clients with up-to-date legislation and guidance as it becomes available. • Ensures quality performance for key/managed projects. • Manages project budgeting/forecasting functions. • Identifies and recognizes out of scope activities in a contract in a timely manner and liaises with other departments to follow through on all aspects of contract modifications. • Collaborates with business development in pricing a

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