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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

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

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 e

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

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

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

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

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

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. An exciting and challenging opportunity has arisen to join th

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; applies query resolution tech

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. Our Clinical Development model brings the customer and the patient to the center of everything

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. Senior-level experience in clinical trials, clinical research, or medical diagnostics. Vista Health is seeking a commercially minded and str

Oncology Clinical Trial Manager position available, home-based UK (single-sponsor aligned). As a leader in our research department, you will collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery of clinical trial outcomes.

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-

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

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.

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

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 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

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

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

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. Ensure compliance with applicable regulations globally and by region, including adherence to Good Clinical Practice (GC

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

If you are a UK registered Pediatric Nurse, who is passionate about patient care, wanting to enhance your primary care clinical skills and develop your clinical potential then please do reach out to learn more. Pediatric Nurse (temporary contract) - Clinical Trial Sites in Bristol, United Kingdom. P

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

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.

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

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

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.

Strong knowledge of clinical drug development process, including trial design, GCP, regulatory processes, and clinical project management. Supports other C-ISRC and Clinical Development projects and activities as. The Central Integrated Scientific Review Committee Lead (C-ISRC Lead) plays a key role

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

Cygnet Hospital Godden Green .As an activities coordinator you will providing activities to patients across various service lines within the hospital.Your main job role will be to co-ordinate, design and deliver a co-produced, personalised activity programme, that is occupationally balanced, r

Familiarity with various clinical trial designs, including accelerated approval, pivotal, and breakthrough pathways. Roche’s Clinical Development organisation is structured by therapeutic area and is responsible for developing and executing the late development (Phase II – III) clinical strategi

Join Psicon’s ADOS Booster Program – Advance Your Clinical Career. Must be Occupational Therapist, Educational psychologist, Speech and Language Therapist or Clinical Psychologist to be considered.

Typically, a Clinical Advisor could earn anywhere.

This is an exciting time to join the MSE group as Clinical Fellow.

As a Clinical Pathologist, the majority of your duties involve but are not limited to, providing clients with diagnostic evaluation in the area of clinical pathology and providing necessary follow-up consultation. Board certification in clinical pathology - American College of Veterinary Pathology (

In collaboration with the Head of Clinical Logistics, participate in the review and improvement of clinical operational systems and processes, enabling continual improvement in line with the company's quality improvement strategy. Working with the Head of Clinical Logistics and the Facilities Manage

This is an exciting time to join the MSE group as Clinical Fellow.

The Advanced Clinical Practitioner (ACP) will work within a primary care hub, delivering expert clinical assessment, diagnosis, treatment, and ongoing management of patients. Job Opportunity: Advanced Clinical Practitioner (ACP). The role involves a mix of clinical care, leadership, education, and s

The approach focuses on meeting the needs of the young person to ensure effective clinical practice and brief therapeutic interventions, and to reduce risk in order to have a stabilising impact within a containing approach.

This is a meaningful opportunity to make a lasting impact while advancing your clinical skills in a supportive environment. At least two years of clinical experience with children and families.

Provide clinical supervision (including case management) to Step 3 clinicians, ensuring supervisees work safely and professionally. Assist the clinical leadership team in supporting and developing the High Intensity part of the service. Experience of offering clinical supervision to other therapists

Provide strong leadership and access to clinical expertise across the area with a significant contribution to direct care. Act as a clinical leader supporting the development of best practice in line with trust policy and NICE guidance. Dedicated, compassionate mental health professional with clinic

As a Regional Clinical Development Nurse at Barchester, you'll lead, support and continuously improve the clinical governance and quality of care for residents in eight of our care homes throughout Essex and Basingstoke. Whether you're organising new training, helping attract key senior clinical sta

Senior Manager, Global Clinical Affairs. This role is pivotal in designing and managing robust in vitro and clinical programs that meet regulatory requirements and drive product innovation.