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Clinical Trial Supplies Manager Role: Collaborate with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers Proactively defines, plans, and communicates the clinical supply chain strategy in support of global clinical studies Responsible for identifyi

Proven experience supporting Phase I-III clinical trials in Pharma or CRO settings. Senior Clinical Trial Management Associate. Join Our Team as a Senior Clinical Trial Management Associate and Drive Life-Changing Oncology Research.

Works with Clinical Program Managers and Global Clinical Trial Leads to manage the European component of global clinical trials and/or the entire process of a local clinical trial, with the ability to identify issues and adapt to changes. May serve as a resource for others within the company for cli

Parexel is currently registering interest for Associate Clinical Operations Leaders (Senior Clinical Trial Specialists) to join us in the UK, dedicated to a single sponsor.

Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead’s products. Un

Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. Parexel is seeking an experienced Clinical Trial Manager to join one of our key sponsors in the UK as a Clinical Study Leader. Supports compliance with

Working closely with Clinical Development, Clinical Operations, and external clinical trial site staff, the clinical scientist will ensure scientific integrity and operational excellence in AIRNA’s clinical trials. The Clinical Scientist supports the design, execution, and analysis of clinical tri

Support the pharmacy clinical trials team, for all education and training and clinical governance to new and active clinical trials. Work closely with the research team and provide highly specialist advice in prescribing and management of adverse events of IMP in line with the clinical trial protoco

Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience. CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close ou

Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines. Global Clinical Project Manager - Vendor Management Expert - Novartis Dedicated (home-based in Europe). Our Clinical Trial Managers work from their

Lead clinical supply strategies in alignment with study design, corporate goals, and regulatory standards. Provide input on clinical protocols, influence study timelines, and advise on country selection. Strong background in the pharmaceutical/biotech industry with significant clinical supply chain

The CTA plays a vital role in supporting the Clinical Study Team (CST) to ensure the successful execution of clinical trials across all phases. Strong knowledge of FDA regulations, ICH/GCP guidelines, and clinical trial processes. KPS Life is looking to recruit a Clinical Trial Associate (CTA) on a

Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. We translate unique clinical, medical affairs and commercial insights into outcomes to address

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

Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines. May perform assigned administrative tasks to support

Clinical Trial Manager - Oncology. Oversee clinical trial budgets (up to 25%) including forecasting and variance reviews. Direct CROs and clinical vendors.

Roles within the Clinical Trial Management job family are responsible for overseeing the development, coordination, and implementation of Phase 1 clinical research studies at the organizations facilities. For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes; conducts

Works with Clinical Program Managers and Global Clinical Trial Leads to manage the European component of global clinical trials and/or the entire process of a local clinical trial, with the ability to identify issues and adapt to changes. Thorough knowledge and understanding of FDA and EU Regulation

It has been set up to provide a single interface for those wishing to conduct clinical trials within the partner institutions, and to ensure that there are common, efficient processes for the set up and administration of clinical trials. Assist the Quality Team to ensure that all trials sponsored or

Senior-level experience in clinical trials, clinical research, or medical diagnostics. This is a unique opportunity to build and grow our UK clinical research business, positioning Vista Health as a leading provider of clinical trials nationwide. Vista Health is seeking a commercially minded and str

Strong knowledge of clinical drug development process, including trial design, GCP, regulatory processes, and clinical project management. Assists in the development of high-quality protocols and other clinical documents by addressing C-ISRC processes/workflow related questions. Supports other C-ISR

Oncology Clinical Trial Manager position available, home-based UK (single-sponsor aligned). We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. As a leader in our research department, you will collaborate with cross-functional teams, manage site relati

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Communicate and collaborate on globa

In this pivotal role, you'll lead and oversee clinical trials. Senior Clinical Trial Manager UK. Lead and coordinate all clinical trial activities in compliance with GCP and regulatory guidelines.

Proactively defines, plans, and communicates the clinical supply chain strategy in support of global clinical studies. For more information, or to apply for this Clinical Trial Supplies Manager, please contact the Key Accounts Team. CK Group are recruiting for a Clinical Trial Supplies Manager to jo

Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in the performance of clinical trial management activities. Candidates should expect to have an intensive training period and show the desire a

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career

They are responsible for formal clinical trial monitoring to ensure trials are conducted, recorded and reported in adherence with the Protocol, SOPs and relevant Regulatory Guidance such as Good Clinical Practice. Ensure clinical trials are conducted, recorded and reported in adherence with the Prot

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Compile and maintain project-specifi

Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials. Work with the clinical trial management staff to support

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred;. Project Manager/Clinical Tria

Essential Functions of a Clinical Trial Assistant (CTA)*** Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project time

CPL Life Sciences are partnering with a well renowned CRO who are seeking an experienced Clinical Trial Manager. Experience of direct clinical trial management. Trial Management team to focus on a number of studies across phases II-III.

We are seeking an experienced Clinical Trial Manager to join a London-based biotech and lead the planning, execution, and delivery of clinical trials. Lead the design, start-up, and execution of clinical trials, ensuring projects are completed on schedule, within scope, and aligned with budgetary ex

Strong knowledge of clinical drug development process, including trial design, GCP, regulatory processes, and clinical project management. Manages C-ISRC Review process for approximately 100+ clinical documents. Assists in the development of high-quality protocols and other clinical.

This position is responsible for creating and maintaining supply strategies for investigational products across global clinical studies. The role requires proactive collaboration, strategic planning, and operational excellence to ensure timely delivery of quality clinical supplies while navigating c

Are you looking for an employer who can offer you opportunities for growth and development in your clinical career- All whilst working within a friendly multidisciplinary team in a rewarding education setting? Do you want to have opportunities to participate in research projects, special interest

We are seeking an experienced Clinical Trial Manager to join a London-based biotech and lead the planning, execution, and delivery of clinical trials. Lead the design, start-up, and execution of clinical trials, ensuring projects are completed on schedule, within scope, and aligned with budgetary ex

Strong knowledge of clinical drug development process, including trial design, GCP, regulatory processes, and clinical project management. The Central Integrated Scientific Review Committee Lead (C-ISRC Lead) plays a key role in the review and approval of clinical documents across therapeutic areas

South Thames vascular access clinical training opportunity.

Work with Clinical Governance Sub-Committee chair and trustees. Develop and oversee clinically appropriate Policies, Procedures and Processes including safeguarding, GDPR, therapist accreditation and CPD needs. Promote a culture of learning within the clinical team, ensuring therapists are up to dat

The Home manager Laxmi has a clinical background and healthcare experience and been with Bupa just over 3 years, we also have a number of long-standing staff 20 years plus.

Clinical Trial Protocol, Clinical Development Plan, Concept Sheet, Investigator Brochure, and Clinical Data Review) in alignment with other process SMEs/owner. The Director Clinical Processes & Solutions, in close collaboration with Process, Risk & Surveillance (PRS), is accountable for the CD end-t

Acting as a clinical and scientific expert, you will provide leadership and oversight for clinical deliverables across late-phase clinical programs and global trials. Oversee ongoing scientific and clinical review of trial data in close collaboration with medical monitors, data management, and biost

Experience in clinical trial design and methodology. Understanding of digital tools in clinical trial execution. CPL Life Sciences are seeking an experienced Clinical Protocol Manager/Director to provide strategic, scientific, and operational leadership across clinical development programs.

May be assigned to lead clinical trial(s) as Clinical Scientific Lead and provide leadership and guidance for all clinical aspects of a clinical trial in close collaboration with the assigned medical monitor and/or CDMD. Clinical deliverables may include the clinical development strategy for assigne

Clinical Trainer (Coastal) Temporary up to 14 months.

Work in support / conjunction with the Senior Clinical Trials Coordinator/Clinical Trials Practitioner/Research Nurses to manage a number of trials, ensuring trial protocols and governance are strictly adhered to, managed within current UK clinical trial directives & regulations in accordance with I