Latest Clinical Project Management jobs in Oxford (page 2)

23 Clinical Project Management Jobs in Oxford - page 2

Senior Clinical Data Manager - single sponsor Fortrea - Maidenhead, United Kingdom Provides CDM leadership for one or more assigned projects or indications dependent on size and scale of the project. Takes global accountability and serves as the second line of contact at the project... Competitive 6 days ago
Clinical Trial Manager UK, In Vitro Diagnostics reading, england, United Kingdom Manage Clinical Research Organization (CRO) interactions, including sponsor oversight of relevant functional activities (e.g., study management, monitoring, site management, project master files, and data... 3 days ago
Manager, Clinical Operations reading, england, United Kingdom IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data... 8 days ago
Clinical Trial Specialist Consult - Maidenhead, United Kingdom • Track key project milestones, compare actual progress with planned activities and timelines, and communicate any issues or changes to relevant stakeholders and management in accordance with company procedures... 10 days ago
Experienced Clinical Research Associate, Sponsor Dedicated reading, england, United Kingdom Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution... 8 days ago
Biostatistician II reading, england, United Kingdom ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment... 11 days ago
Sr Site Enablement Solutions Project Lead (m/w/d) IQVIA - Reading To perform the Site Enablement Solution Project Lead job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the... 13 days ago
Senior Regulatory Medical Writer, sponsor-dedicated Fortrea - Maidenhead, United Kingdom You will leverage your experience to manage writing projects, coordinate and collaborate with stakeholders, steer discussion, drive consensus and facilitate decision-making to propel the document development... Competitive 13 days ago
Clinical Vendor Program Manager - Novartis Dedicated reading, england, United Kingdom Manage and documents vendor performance issues and risk and escalate it to VSE, as needed Coordinatesvendor deliverables across VSE during study start-up Extensive working experience and knowledge of the... 20 days ago
Senior/Principal HTA Statistician Wokingham, England, United Kingdom By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates... 24 days ago

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