Your Role : as an Associate Director, Trial Clinical Delivery Lead, where you will play a pivotal role in ensuring the success of Phase I-IIIb Clinical Development studies. You will oversee study, country, and site-level activities, serving as the primary contact for site management and operational issues. You will provide strategic direction and leadership for Clinical Site Leads (CSLs), ensuring quality and performance oversight. You will foster data-driven planning and accountability among internal and external partners. You will implement operational excellence strategies, leveraging expertise from Global Development Operations, facilitate timely issue escalation, and promote solution-oriented thinking within study teams. You will collaborate on patient-directed recruitment strategies and integrate insights from stakeholders to enhance study design. You will also lead process improvement initiatives and ensure adherence to timelines, budgets, and quality standards. This position belongs to a global team and can be based in any city in Spain.
Who You Are :
* Graduate degree in Medical or Life Sciences, or equivalent.
* Clinical operations experience across Phases I-IIIb.
* Expert knowledge of clinical development principles and regulatory environments (e.g., ICH GCP).
* Desired experience in Oncology, Neurology, or Immunology.
* Over 10 years in clinical research within CRO, pharma, or biotech, including site management and study planning.
* Strong skills in adaptability, critical thinking, communication, and analysis.
* Ability to work independently and manage multiple tasks effectively.
* Proficient in risk assessment and problem-solving.
* Fluent in English and local language; travel may be required (up to 20%).
Delivery Lead
* Madrid, Kingdom Of Spain, ES
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