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Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis) Are you an experienced Vendor Management professional looking to make an impact in global clinical trials?We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor Department, dedicated exclusively to Novartis. In this role, you ll become an expert in Vendor Management for global clinical trials across all phases (Phase I–IV), ensuring seamless execution from study start-up through close-out.What We’re Looking ForTo excel in this role, you should bring:Global Clinical Project Management experienceStrong Vendor Management expertise: Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment & Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors)Deep understanding of clinical operations processes and vendor service categories.Excellent project management skills to drive efficiency and collaborationStrong communication and influencing abilities to partner effectively across functions.Proven ability to manage risk and performance issues in a fast-paced environmentWhat You’ll DoAs a Global Clinical Project Manager - Vendor Management Expert, you will be responsible for ensuring vendor deliverables are met with quality and efficiency at the trial level. Your key responsibilities include:Vendor Oversight & Coordination – Manage vendor activities across the study lifecycle, ensuring timely and high-quality deliverables.Study Start-Up Support – Oversee vendor deliverables during study initiation, ensuring smooth onboarding and activation.Risk & Performance Management – Track vendor performance, identify risks, and escalate issues as needed.Site Readiness & Activation – Drive vendor activities to support site activations and ensure study milestones are met.Study Close-Out – Coordinate vendor deliverables that support Database Lock and study closure.What You’ll DeliverVendor service excellence at the study levelVendor onboarding and performance trackingKPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectivenessSite readiness monitoring and documentationRisk mapping with contingency planningVendor cost control and oversightPlease note this role is not eligible for the UK visa sponsorship.This is an exciting opportunity to play a critical role in global clinical trials, ensuring vendor excellence and operational success. If you’re ready to take on a high-impact role with a leading sponsor, we’d love to hear from you!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

Job overview Are you a Clinical (Project) IRT Manager with a passion for vendor excellence and study startup success? We’re looking for a Vendor Startup Manager (VSM) to join our Single Sponsor Department, dedicated exclusively to Novartis. In this role, you’ll bring technical expertise to accelerate vendor service delivery during the critical startup phase of global clinical trials. What We’re Looking For To thrive in this role, you’ll bring: ✅ Strong vendor management skills and deep knowledge of clinical trial startup processes ✅ Strategic thinking and the ability to assess risk and implement contingency plans ✅ Experience with vendor contracting, budgeting, and onboarding ✅ Excellent communication and collaboration skills across internal and external stakeholders ✅ Hands-on experience with tools like IRT, UAT (User Acceptance Testing) and UVP (Unified Vendor Portal) What You’ll Do As a Vendor Startup Manager, you’ll be the go-to expert for vendor service categories during study startup. Your key responsibilities include: Protocol & Specification Review – Ensure vendor input is reflected in final study specs Study Specification Worksheet (SSW) – Support vendor selection and bid process Vendor Kick-Off & Onboarding – Lead meetings and ensure readiness for DB go-live Budget & Contract Support – Review quotes and assist with negotiations Risk Mapping & Contingency Planning – Proactively identify and mitigate startup risks Performance Oversight – Monitor vendor delivery and escalate issues as needed UAT Execution – Conduct robust testing and design for IRT systems Collaboration – Partner with TVMs, VALs, Procurement, and QA to drive startup success What You’ll Deliver Accelerated and high-quality vendor startup Vendor risk maps and performance tracking Audit-ready documentation and compliance Continuous improvement and best practice sharing Expertise in key service categories like Central Labs, Imaging, and Diagnostics This is a high-impact opportunity to shape the success of global clinical trials from day one. If you’re ready to lead vendor startup excellence in a dynamic, sponsor-focused environment—we’d love to hear from you! This position is not eligible for UK VISA Sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

Location: UK, home-basedDepartment: Clinical OperationsAs a Senior Local Trial Manager (LTM) at IQVIA, you’ll play a pivotal role in accelerating the delivery of innovative therapies to patients. You’ll lead the planning, execution, and ov

Clinician (Neurologist, Alzheimer's study) // Japanese-speaking, luton, bedfordshire. Hobson Prior is seeking a Japanese-speaking freelance clinician to support clinical trial activities in Alzheimer's Disease.

The Clinical Trial Assistant will perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Minimum 6-12 months clinical trial assistance experience. IQVIA are seeking

May assist in the review of study-related documents as they relate to the supported clinical trials as delegated by the Regional Clinical Study Manager (e. Applies knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager. Acquires regional study man

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. Clinical Trial Manager, Clinical Operations Leader, Lead CRA

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Join to apply for the Clinical Trial Manager - Oncology - EU - Remote role at Worldwide Clinical Trials. Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role. We’re Worldwide Clinical Trials, a global midsize CRO that pushes boundaries, innovates and invents because the

Applies knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager. May assist in addressing routine study questions from clinical trial sites. Oversees multiple aspects of clinical trial conduct at the regional level, including feasibility, study sta

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Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical tria

Ensure accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical trial

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The aCTM will be part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based A

Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills. Leads the development of the clinical trial strategy and delivers the clinical ope

As a Clinical Trial Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Role: Clinical Trial Manager - FSP. Lead and manage the conduct of clinical trials from start-up to closeout in accordance with ICH-GCP and

Sales Executive – Pharmacovigilance/Clinical Trial IT Solutions (Life Sciences). Reporting to our VP of Sales & Marketing in Paris, you will be responsible for selling our Pharmacovigilance and Clinical Trials solutions to clients in the life sciences and healthcare sectors located in Europe, and

The Clinical Lead works closely with the Nurse Lead and the Care, Quality and Compliance Manager to ensure the service maintains its high levels of clinical documentation, auditing and regulatory compliance, and works alongside the team the team to ensure that best practices are followed, both for c

The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. Ensure compliance of clinical trials with national and international regulatory requirements and co-monitoring the assigned

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Previous experience in UK clinical trial management. CK Group are recruiting for a Clinical Study Manager to join a company in the Pharmaceutical industry, at their site based in Welwyn Garden City, on a contract basis for 6 months. Drive operational excellence by developing operational plans, creat

Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and managemen

Previous experience in UK clinical trial management. CK Group are recruiting for a Clinical Study Manager to join a company in the Pharmaceutical industry, at their site based in Welwyn Garden City, on a contract basis for 6 months. Drive Operational Excellence by developing operational plans, creat

We’re now looking for a warm, enthusiastic, and dedicated individual to join our award-winning team as a Clinical Lead. Your focus as Clinical Lead will be to support the Home Manager across all aspects of Home Management, providing a safe, caring, stimulating and homely environment for residents

To contribute to workforce planning, ensuring clinical engagement with local and national workforce planning processes. To support the use of clinical skills training and simulation (where appropriate/applicable), stressing the importance of teamwork and human factors. To contribute to workforce pla

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Visa sponsorship is not available for this role.Applicants must already have the right to work in the UK.Continued Process Verification (CPV) / Process Validation.Technical Associate II, MSAT (CPV / Process Validation SME).Stevenage, UK (occasional London).Fixed shifts also available if preffered.A

Carry out clinical coaching with both new and existing staff following training to ensure a smooth and consistent learning journey. Carry out daily clinical audits and provide constructive and informative feedback via the PRS systems on new and existing staff member. Job Description What you'll be

Ideally you will have at least 1-2 years experience of supporting Clinical Trials in the UK. Much of the work will involve complex oncological clinical trials, providing valuable opportunities to develop your skills and expertise. This is a great opportunity to gain hands-on experience in clinical r

Partner with other clinical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program. You will provide clinical and scientific oversight and support for multiple, global Phase 1 - 4 clinical trials

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Clinical Deputy ManagerSt Mark’s Care Home, 110 St Marks Road, Maidenhead, Berkshire, SL6 6DN.

Clinical Lead - Pre Assessment - Circle Health Group. Sign in to set job alerts for “Clinical Lead” roles. Clinical Specialist Physiotherapist - Specialist Medicine.

Join our client, a leading organisation in the pharmaceutical industry, as a Contract Clinical Operations Lead in! This is an exciting opportunity for a passionate professional looking to make a difference in clinical trial delivery. You are a dynamic individual motivated by the mission to innovate

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Applications are invited for the post of Clinical Fellow Higher (ST6+) in Paediatric Intensive Care (PICU) and Paediatric Retrieval (PaNDR) at Cambridge University Hospitals NHS Foundation Trust to commence 05 November 2025 for 12 months in the first instance. It is the only PICU in the East of Engl

Applications are invited for the post of Clinical Fellow Higher (ST6+) in Paediatric Intensive Care (PICU) and Paediatric Retrieval (PaNDR) at Cambridge University Hospitals NHS Foundation Trust to commence 05 November 2025 for 12 months in the first instance. It is the only PICU in the East of Engl

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Clinical interpretation skills, stakeholder management skills. Our team provides expert communications leadership to drug projects, crafting clinical-regulatory documents that align with project strategies and regulatory requirements. Your role will involve developing communication strategies, optim