Senior Project Manager - EMEA - FSP
Ontdek meer
Over deze vacature
Senior Project Manager - EMEA - FSP
To your colleagues or friends
Volver a los resultados de búsqueda
Standard (Mon-Fri)Office
Join Us as a Senior Project Manager in FSP - Make an Impact at the Forefront of InnovationThe Senior Project Manager serves as the client embedded Project Lead and primary sponsor contact and is accountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. The Senior Project Manager establishes and communicates customer expectations to the project team with minimal direction and ensures that escalation pathways are adhered to internally and externally. The role involves leading the cross functional project team to meet or exceed deliverables and managing project(s) of increasing complexity (such as but not limited to: multi-service, multi/region/country, therapeutic complexity, financial scope). What You'll Do:As a client-embedded Project Manager serving as the primary point of contact between study teams, stakeholders and CRO/vendors, ensuring effective coordination and communication across all parties. Responsible for the end-to-end delivery of clinical studies through cross-functional project leadership, ensuring alignment with sponsor processes, tools and performance measures. Oversees study timelines, budgets and CRO/vendor deliverables, including management of out-of-scope activities and contract modifications. Leads risk management and mitigation activities, ensuring proactive issue identification, escalation and resolution.
Maintains clear communication pathways across study teams, sponsors and stakeholders to support efficient, high-quality study execution in compliance with regulatory requirements and ICH-GCP standards.Education & Experience Requirements: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years’) Biotech experience is a plus.
Rare disease, Auto-immune, and/or oncology clinical trial background is a plus.Knowledge, Skills, Abilities: Technical and systems competency, such as computer skills, to include effective use of systems and applications such as Microsoft Outlook, Word, Excel and PowerPoint, as well as experience with tools and systems for managing clinical studies (MS Project, CTMS, TMF, IWRS, eCOA, eCRF databases, etc) Ability to delegate and effectively prioritize workload and resources for project team members in a frequently changing environment Effective oral and written communication and presentation skills Proactive, solutions oriented and adaptable in changing priorities and situations In-depth therapeutic area knowledge and clinical development guidelines and directives Advanced knowledge of the key principles of cross functional project management (Time, Quality, Cost) Effective interpersonal including the ability to lead, motivate and coordinate cross-functional project teams Strong customer service skills with the ability to proactively address and prioritize expectations Good judgment and decision making skills and proven ability to apply critical and analytical strategic thinking skills to manage complex/ambiguous situations Strong negotiation skills with ability to influence others and achieve results, including a cross cultural awareness Strong financial acumen with the knowledge and ability to minimize risk by proactively managing and adjusting budgets/forecasts/resources Ability to work independently with minimal supervision.Working Conditions and Environment: Work is performed in an office/ laboratory and/or a clinical environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Personal protective equipment required such as protective eyewear, garments and gloves.Why Join Us?When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.Apply today to help us deliver tomorrow’s breakthroughs.
Recibe notificaciones de trabajos similares
Recibirás actualizaciones una vez por semana
Project Manager/Sr Project Manager - FSP - NIS experience
Step into the role of Senior Project Manager and lead cross-functional teams to deliver high-quality, timely, and cost-effective projects. Serve as the primary sponsor contact, manage vendor relationships, and ensure compliance with clinical and regulatory standards. Join Thermo Fisher Scientific and help drive impactful, innovative solutions in a dynamic environment.
Project Manager/Trial Lead - FSP - EMEA
Embrace the opportunity to become a Project Manager and lead cross-functional teams to deliver high-impact clinical trials across EMEA. Drive project success from planning to execution, ensuring quality, compliance, and customer satisfaction. If you excel in project management and thrive in dynamic environments, this is your opportunity to make a difference.
Join us as a Senior Clinical Team Manager within the Hematology/Oncology team, where you will oversee clinical deliverables and ensure project milestones are met. Lead a team to manage clinical operations and quality, leveraging your experience in clinical trial management. Ideal for candidates with strong leadership and expertise in clinical research.
Senior CTM, Internal Medicine (Dermatology, Nephrology, Cardiovascular, Women's Health, GI, Immunology, Rare Disease)
Step into the role of Senior Clinical Trial Manager within our Internal Medicine Therapeutic Business Unit. Lead clinical operations, ensure compliance with ICH GCP, and manage complex studies across multiple therapeutic areas. Join Thermo Fisher Scientific and make a meaningful impact in advancing clinical research.
Regulatory FSP Director CMC Lead - EMEA
Step into the role of Director, Regulatory Affairs — CMC FSP and provide senior technical and operational leadership for CMC regulatory services. Lead teams, advise clients, and drive quality performance across key projects in a dynamic, collaborative environment at Thermo Fisher Scientific.
Regulatory Affairs Senior Specialist - Trial Transparency Liaison - FSP EMEA
Step into the role of Senior Regulatory Affairs Specialist and provide strategic regulatory guidance for global clinical trials. Lead transparency activities, manage clinical trial disclosures, and collaborate with cross-functional teams to ensure compliance with evolving regulations. Join us to make a meaningful impact in the pharmaceutical and biotech industry.
Clinical Team Manager FSP - Country Study Manager
Step into the role of Clinical Team Manager and lead the operational delivery of clinical trials within a dynamic, evolving environment. Oversee study planning, site selection, vendor management, and ensure high-quality execution of clinical studies. Join Thermo Fisher Scientific and help drive impactful research in a collaborative, global team.
FSP RA - Client Dedicated - CMC Project Manager
Ready to make an impact as a Regulatory Affairs CMC Project Manager? Join our team to lead CMC development for therapeutic antibodies, drive project success, and provide regulatory expertise from preclinical stages through product optimization. Collaborate globally and play a key role in advancing innovative medicines.
We are currently hiring a Senior Contract Specialist to manage the preparation, negotiation, and finalization of investigator contracts across Germany, Austria, and Switzerland. You will ensure compliance, risk analysis, and effective collaboration with internal and external stakeholders. Ideal candidates bring significant contract law expertise and experience in pharmaceutical contract management.
Los solicitantes de empleo también vieron
Nos aseguraremos de que las personas con discapacidades reciban adaptaciones razonables para participar en el proceso de solicitud de empleo o entrevista de trabajo, para que puedan ejercer las funciones de trabajo esenciales y recibir otros beneficios y privilegios del empleo. Comuníquese con nosotros para solicitar una adaptación.