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We are seeking a dynamic and experienced Nurse Manager to join our clinical research site leadership team. This pivotal role supports the Site Manager in driving operational excellence, including profit and loss optimisation, while ensuring the delivery of high-quality, safe, and compliant clinical research services. You will lead nursing activities across all phases of clinical trials in accordance with ICH/GCP guidelines and local regulatory requirements. Key Responsibilities Strategic & Operational Leadership • Collaborate with the Site Manager to optimise site performance, resource allocation, and financial outcomes., • Contribute to strategic planning and execution of site goals, KPIs, and business development initiatives., • Oversee nursing activities from trial initiation to close-out, ensuring adherence to ICH/GCP and protocol-specific requirements., • Coordinate with sponsors, CROs, and internal stakeholders to ensure smooth trial conduct and timely data collection., • Ensure the clinical area operates in full compliance with regulatory standards, SOPs, and ethical guidelines., • Lead internal audits and support external inspections, implementing corrective actions where necessary., • Recruit, train, and supervise nursing staff, ensuring competency in clinical trial procedures and patient safety., • Promote a patient-centric approach, ensuring informed consent, dignity, and comfort throughout the research process., • Act as a clinical resource for complex procedures, protocol interpretation, and emergency response. Qualifications & Experience • Registered Nurse (RN) with active license to practice., • Minimum 3 years of experience in clinical research within a leadership role, • Strong knowledge of ICH/GCP guidelines and clinical trial operations., • Proven ability to manage teams, budgets, and operational metrics., • Excellent communication, organisational, and problem-solving skills.

Clinical Trial Pharmacist, sheffield, south yorkshire.

Oxford Global Resources is hiring a Clinical Study Lead (IVD experience is a must) for temporary maternity leave.As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols, investigator

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

You will be central to the delivery of clinical trials, ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Home Office regulations. You’ll play a key role in supporting the safe and effective management of Investigational Medicinal Products (IMPs) across

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. Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role;. Clinical Trial Manager

You will be central to the delivery of clinical trials, ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Home Office regulations. Clerkenwell Health is an innovative and leading Research Organisation specialising in the delivery of scientifically grounded

Plan logistics and resource usage for clinical trials, including the allocation of staff, equipment, and materials, to ensure that trials are conducted smoothly and without delays. Oversee the development, coordination, and implementation of Phase 1 clinical research studies at the organization's fa

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

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

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

In this pivotal role, you'll lead and oversee clinical trials. Deep understanding of ICH/GCP and global clinical trial regulations. Senior Clinical Trial Manager UK.

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

Pediatric Nurse (temporary contract) - Clinical Trial Sites in Bristol, United Kingdom. ProPharma are looking for Pediatric Nurses to support clinical trials sites in the United Kingdom with patient home visits. No prior clinical trial experience needed as training will be undertaken on the role.

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

You will be central to the delivery of clinical trials, ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Home Office regulations. You’ll play a key role in supporting the safe and effective management of Investigational Medicinal Products (IMPs) across

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

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. Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial

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

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. Candidates should expect to have an

The CTA plays a vital role in supporting the Clinical Study Team (CST) to ensure the successful execution of clinical trials across all phases. KPS Life is looking to recruit a Clinical Trial Associate (CTA) on a fixed-term contract, 1 FTE. Clinical Trial Support: Coordinate and support study start-

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

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

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

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

Oncology Clinical Trial Manager position available, home-based UK (single-sponsor aligned). In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a l

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

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Our global Clinical Operations colleagues within our PPD clini

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. Candidates should expect to have an

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

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. Clinical Trial Managers with expertise in Nephrology are welcome to continue to work in their area of expertise or t

Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role. Senior / Clinical Trial Manager - Oncology - Europe - Remote. Provide leadership and direction to the clinical site management team from study start through closure.

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.

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

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.

We are seeking an experienced Clinical Trial Manager to join a London-based biotech and lead the planning, execution, and delivery of clinical trials. Minimum of 8 years in clinical trial management across pharma, biotech, or CROs. Lead the design, start-up, and execution of clinical trials, ensurin

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.

You will be central to the delivery of clinical trials, ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Home Office regulations. Support training and supervision of junior staff, and deliver clinical trial training across teams. If you're passionate abou