Experteer Overview ¿Es este el siguiente paso en su carrera? Descubra si es el candidato adecuado leyendo la descripción completa a continuación. As Global Study Manager, you will support delivery of clinical studies from CSP development through CSR and archiving. You’ll work cross-functionally to keep studies on time, within budget, and to quality standards, coordinating with GSD/GSAD and external partners. You will lead study document preparation, sponsor and CRO interactions, risk management, and TMF quality assurance. This is a globally connected, remote-friendly role with a focus on compliant, efficient study execution and continuous improvement. You’ll contribute to budget oversight and vendor management as part of a dedicated EMEA team.Compensaciones / Incentivos• Lead and contribute to delegated study documents (e.g., informed consent, master clinical study agreement) and external service provider documents• Maintain and facilitate interactions with internal and external functions including CROs to achieve study objectives• Contribute to planning and conduct of internal and external meetings (Investigators'/Monitors' meetings)• Ensure supply of Investigational Product and study materials via Clinical Supply Chain or external providers• Identify risks/issues and develop mitigation/action plans• Ensure study documents under GSM scope are complete and QA-verified in Trial Master File• Support GSD/GSAD with budget management (invoice reconciliation)• Adhere to global clinical processes, ICH/GCP, and compliance manuals to ensure inspection readiness• Support overall project management per delegation; oversee CRO Project Manager for outsourced studies with appropriate oversight• Take on non-drug project work in process improvements or improvement projectsResponsabilidades• University degree (or equivalent)• At least 3 years’ experience in pharmaceutical industry or similar organization• Knowledge of xcskxlj clinical development processes and various phases• Excellent knowledge of ICH/GCP• Strong communication and relationship-building skills, including external service provider management• Good project management skills; ability to collaborate and work independently; demonstrated leadership• Computer proficiency and advanced day-to-day tools• Fluent English (verbal and written)Requisitos principales• remote work• flexible work arrangements• health and welfare benefits• global collaboration and learning opportunities• access to collaborative tools• remote-friendly culture

📌 Global Study Manager - Single Sponsor dedicated (in EMEA) (Madrid)
🏢 Talent
📍 Madrid