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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

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. 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

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

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

Strong knowledge of clinical drug development process, including trial design, GCP, regulatory processes, and clinical project management. Key outcomes are high-quality concept sheets, protocols and clinical development plans. Manages C-ISRC Review process for approximately 100+ clinical documents.

We are seeking an experienced Clinical Trial Manager to join a London-based biotech and lead the planning, execution, and delivery of clinical trials. Responsibilities:Lead the design, start-up, and execution of clinical trials, ensuring pro

Clinical trials experience (For Clinical Trial Practitioner applicants). The post holder will be expected to develop specialized skills and knowledge relating to the conduct of clinical trials, the therapies and the relevant disease sites, and to provide patients with information to help them make i

As Clinical Trial Manager you will be responsible for providing support or leading specific activities for the planning, set-up and execution of assigned drug trials which may include: pre/post-POC interventional drug trials, Clinical Pharmacology normal healthy volunteer clinical trials, pre-approv

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

Roles within the Clinical Trial Management job family at the P22 level are responsible for overseeing the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. Impact and Contribution: Roles significantly impact the success of clinical t

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

The aCTM will work 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 path into Clinical Trial Management (CTM). Communi

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

For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes Conducts Source Document Review of appropriate site source documents and medical records Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Knowledge of Good Clinical Prac

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

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

Clinical Trial Manager (Clinical Research Medical Advisor) - FSP - Homebased - UK. 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. Minimum 3

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. Essential Functions of a Clinical Trial Assistant (C

The post will involve the coordination and management of all aspects of a clinical trial that will recruit from NHS community intellectual disability services across three countries (England, Scotland and Northern Ireland). Lead the coordination of the clinical trial and provide strategic, tactical

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

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

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.

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. Communicate and collaborate on globa

Impact and Contribution Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Roles within the Clinical Trial Management job family at the P22 level a

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

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

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.

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

Parexel is beginning to search for an experienced Clinical Trial Manager to join one of our key sponsors in the UK as a Clinical Study Leader. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a dee

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

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

Clinical trials experience (For Clinical Trial Practitioner applicants). The post holder will be expected to develop specialized skills and knowledge relating to the conduct of clinical trials, the therapies and the relevant disease sites, and to provide patients with information to help them make i

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 Trial

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. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career

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 organization's facilities. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor repres

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

As a Clinical Trial Leader you will be leading the global multidisciplinary matrix Clinical Trial Team (CTT) to ensure all trial deliverables are met. As a Clinical Trial Leader you will be leading the global multidisciplinary matrix Clinical Trial Team (CTT) to ensure all trial deliverables are met

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

Roles within the Clinical Trial Management job family at the M24 level are responsible for overseeing all aspects of Phase 1 clinical research studies, collaborating with investigators and operations teams, planning logistics and resources, tracking progress, and ensuring compliance globally and reg

As part of the Clinical Operations team, you will support the execution of global Phase 1–4 clinical trials with a strong focus on oncology and advanced cell therapies. Solid experience in clinical trials, ideally within pharma, CROs, or clinical sites. Senior Clinical Trials Management Associate.

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

To gain working knowledge of the aseptic/QA and clinical trial sections of the pharmacy and therefore be able to work competently and with minimum supervision in any section as and when required to do so. Be able to interpret and work with complex clinical trial and aseptic documents/guidelines. Ase

NHS Jobs is seeking a highly qualified and motivated individual to join our dynamic team as a Lead Pharmacist in Haemato-Oncology Clinical Trials. As the Lead Pharmacist, you will play a pivotal role in our Haemato-Oncology Clinical Trials team. Coordinate and lead pharmaceutical services within the