Senior Clinical Project Manager

Veeda Lifesciences is seeking a Senior Clinical Project Manager based in Europe.

Job overview: The Senior Clinical Project Manager will

lead the successful delivery of high-impact, multi-center clinical trials.

In this full-time role, you will be responsible for managing complex project plans, overseeing budgets, maintaining strong sponsor and stakeholder relationships, and ensuring full compliance with GCP, ICH, and regulatory standards.

Main responsibilities: Owns end-to-end project management for clinical trials, ensuring alignment with study goals and timelines. Develops and maintains key project documents, including the Responsibility Matrix, Project Timelines, Risk Management Plans, Communication Plans, Budget Plans, and Vendor Oversight Plans. Monitors study progress to ensure adherence to timelines, budgets, and quality standards, proactively identifying and resolving issues. Acts as the main point of contact for Sponsors; leads sponsor calls, manages follow-ups, and ensures effective communication. Oversees project financials, including budget tracking, forecasting, and ensuring compliance with contractual terms. Drives process improvements through industry-standard tools and techniques to enhance efficiency and project outcomes. Ensures compliance with internal processes, GCP, ICH guidelines, and all applicable regulatory standards. Provides oversight and performance monitoring for vendors and freelancers to maintain project momentum. Leads and supports the project management team through recruitment, onboarding, training, mentorship, performance reviews, and ongoing development.

Job Requirements: Bachelor’s degree in natural or health sciences, business management, or a related field. Desirable: Postgraduate studies or PMP (Project Management Professional) certification. 8+ years of project management experience in the clinical trial industry, with a proven track record in managing multi-center studies. Strong understanding of ICH-GCP and regulatory requirements. 8+ years of experience of proven leadership, mentoring, and team development abilities. Excellent communication, organizational, and planning skills in English (written and verbal). Ability to work independently and manage multiple priorities in a dynamic environment. Willingness to travel up to 20%, including internationally.

Join us to be part of a multidisciplinary team of highly skilled scientists and healthcare professionals in the forefront of Clinical Research within a friendly work environment.