Global Clinical Study Lead

ICON Strategic Solutions is seeking a Global Study Manager for a permanent, home-based role to deliver global clinical studies with sponsor-dedicated FSP support. You will oversee vendor and country team activities, ensure on-time delivery and budget adherence, and collaborate with internal and external partners to uphold high-quality standards.You will work...

AstraZeneca in Barcelona is seeking a Senior Statistical Programmer II to lead programming deliverables for clinical studies, ensuring quality and timeliness in line with established standards.You will apply expert macro programming, contribute to study teams, and drive best practices while maintaining documentation and regulatory compliance.The role...

Clinical Study Manager - Sponsor Dedicated - Spain, UK, Romania, Bulgaria, Czech Republic - remoteAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment...

The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study...

Novartis is seeking a Vendor Program Head within Vendor Partnerships & Governance (VPG) to lead the Development Unit’s vendor strategy, portfolio oversight, and vendor management across clinical development programs. This senior role partners with DU leadership to align vendor priorities with development milestones and quality expectations. The candidate...

The Global Study Associate (GSA) is a member of the extended Global Study Team, supporting the delivery of clinical studies within Late Development Oncology (LDO) to time, cost, and quality standards. The GSA supports clinical studies throughout their lifecycle, from Clinical Study Protocol (CSP) development and study set-up through maintenance, close-out,...

Summary This role is based in Barcelona Gran Via, Spain. Novartis is unable to offer relocation support. Please only apply if accessible.Novartis operates a Hybrid working arrangement with an expectation of 12 days per month onsite.Strong vendor Quality and Compliance are critical to successful clinical development and inspection readiness. As Vendor...

IQVIA is seeking a Global Study Associate Director to lead a cross-functional study team and oversee outsourced delivery for clinical studies in line with timelines, budget, and quality standards.The role requires ICH-GCP knowledge, strong leadership, and experience in study management across all phases. You will drive planning, risk management, and...

IQVIA is seeking a Global Study Associate Director to lead a cross-functional study team and oversee outsourced delivery for clinical studies in line with timelines, budget, and quality standards.The role requires ICH-GCP knowledge, strong leadership, and experience in study management across all phases. You will drive planning, risk management, and...