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- £41k - £55k per annumEstimated...ICON Strategic Solutions seeks a Senior Clinical Trial Manager to lead non-interventional study operations across multiple European locations. The role combines end-to-end study design, execution, and reporting, with responsibility for managing cross-functional teams and delivering...Suggested
- £51k - £69k per annumEstimated...ICON is hiring a Senior Study Delivery Lead to manage clinical research projects in a sponsor-dedicated model across multiple European locations. The role combines end-to-end oversight of non-interventional and interventional studies, vendor management, and cross-functional...Suggested
- £27k - £37k per annumEstimated...independently manage clinical trial contract and budget negotiations with investigator sites across multiple countries. The role supports study start-up through collaborative stakeholder engagement and efficient agreement execution within compliance frameworks....Suggested
- £45k - £59k per annumEstimated...ICON seeks a Global Study Lead to manage clinical trial projects across multiple European locations. The role involves coordinating project delivery, leading cross-functional teams, and ensuring timely completion within budget and quality standards in a sponsor-dedicated model...Suggested
- £40k - £55k per annumEstimated...ICON Strategic Solutions seeks a Senior Clinical Trial Manager to lead study delivery operations in a sponsor-dedicated model, focusing on non-interventional studies. The role combines cross-functional team leadership with end-to-end management of complex clinical trial design...Suggested
- £34k - £47k per annumEstimated...seeks an Associate II for TMF Operations to review, process, and quality-check Trial Master File documentation across complex clinical studies. This remote role, based in Europe, supports regulatory compliance and document lifecycle management across global teams....SuggestedRemote
- £45k - £58k per annumEstimated...ICON seeks an experienced Risk-Based Quality Management (RBQM) Lead to drive proactive, risk-focused quality oversight across clinical studies globally. The role involves leading RBQM planning, cross-functional collaboration, and ongoing risk management to strengthen quality...Suggested
- £48k - £62k per annumEstimated...clinical trial activities Monitor vendor compliance, effectiveness, and performance using scorecards and KPI metrics Partner with study teams to resolve vendor performance issues and support trial delivery Oversee vendor quality incidents and coordinate corrective...SuggestedRemote
- ...trials across Europe. The role involves independent SAP authoring, study integration support, and cross-functional partnership in a global... ...expertise writing and reviewing Statistical Analysis Plans Ability to work independently with minimal direct oversight Strong R...Suggested
- £46k - £64k per annumEstimated...provide scientific and clinical writing support for late-phase projects, including real-world evidence and peri-/post-approval safety studies. The role involves developing study documents, scientific communications, and quality control across a client account team in a...Suggested
- £40k - £55k per annumEstimated...Clinical Scientist role at ICON focused on Veeva EDC transition and clinical study design. The position involves supporting electronic data capture implementation, conducting trials, analyzing data, and collaborating with cross-functional teams to advance therapeutic development...Suggested
- £60k - £81k per annumEstimated...Oversee project delivery from start-up through closeout, managing cross-functional teams, budgets, and stakeholder relationships to ensure studies meet quality, regulatory, and timeline standards. Responsibilities Lead delivery of Phase I-IV clinical trials from study start...SuggestedOn-site
- £50k - £67k per annumEstimated...sales, or client services experience in pharma, biotech, or clinical research Strong knowledge of peri-approval and post-approval study operations and regulatory standards Excellent communication, negotiation, and stakeholder influence skills Track record of achieving...Suggested