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Job Overview: Project Managers own the operational strategy, determining the most cost effective and efficient means to successfully run and complete projects on time, while maintaining quality, remaining within…
Location: Hybrid (2 days per week in the Central London office) We are seeking a Study Start-Up Project Manager to join our team. In this role, you will work 100% dedicated to a leading global pharmaceutical company,…
We are currently expanding our sponsor-dedicated team in Türkiye and are seeking experienced Project Managers, Study Start-Up , to support our continued growth and future opportunities. This hybrid position is based in…
We are currently expanding our sponsor-dedicated team in Türkiye and are looking for experienced Clinical Supply Project Managers. This hybrid position is based in Istanbul . While this role is for anticipated future…
Summary of Responsibilities: Duties include diverse coordination and administrative tasks and activities. May organize multiple processes, procedures, or programs. Responsible for reviewing and supporting the logistics…
Our FSP team is seeking Project Managers/Sr. Project Managers t o j oin our growing team. This role requires 2-5 + years of global project management experience , with experience in Oncology or Ophthalmology .…
Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post…
📍 London | 2–3 days onsite (hybrid) Are you a regulatory‑focused Study Start‑Up expert who thrives on ownership and compliance? We’re looking for a Study Start‑Up PM to lead country‑level submissions, approvals and…
Job Overview: The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face, continuous learning environment,…
Manages country-level clinical trial start-up for a dedicated sponsor at Fortrea's Bucharest office: regulatory and ethics submissions, local-language informed consents, site/country budgets, contracts, and payment oversight. Requires 4-6 years of clinical research experience, ICH/GCP knowledge, and fluency in the local language and English.
Coordinate regulatory submissions and documentation for clinical studies in a sponsor-dedicated office role, ensuring compliance and smooth workflows.
Coordinate Phase I clinical trials, maintain study documents, track milestones, and manage CTMS/eTMF systems to support first-in-human drug development.
Are you detail-oriented and passionate about supporting clinical research operations? If so, join our team in Munich as a Project Coordinator (Budget & Finance focus) , where you’ll play a key role in enabling…
Job Overview: At times working under the direction of a Project Director, the Senior Project Manager oversees and manages domestic, regional and/or global projects. Responsibilities typically include developing and…
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