You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner. Key Responsibilities - Manage clinical supply strategies within clinical studies whilst ensuring these delivered in a timely and cost-efficient manner
Job Description The Scientist for Clinical Trials - Oncology - Thoracic (Sr. Manager)(non-MD)is responsible forproviding support ofscientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio. Job Responsibilities - Clinical development professional maintaining current scientific and clinical...
Global Study ManagerDuration - 12 months (interim)Location - RemoteInside IR35Rate - £500.00 (Umbrella) or £402.00 (PAYE) per dayThe Global Study Manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance. The exact accountabilities will differ depending on the exact nature of the clinical program, so a high degree of flexibility is...
Clinical Trial Manager – UK | Advanced Clinical (FSP Model) Oncology focused Advanced Clinical is seeking an experienced Clinical Trial Manager to join our UK-based Functional Service Provider (FSP) team. This role will support global clinical studies and requires strong operational, vendor management, and monitoring oversight experience. Responsibilities include: - Managing external vendors...
Contractor Global Studies Asset Manager (GSAM)Location: Hertfordshire (Hybrid)Contract RoleWe are seeking an experienced Global Studies Asset Manager (GSAM) to support the operational delivery of a portfolio of clinical studies within a therapeutic or disease area. In this role, you’ll drive high‑quality execution, partner with global and country teams, and collaborate closely with CROs to ensure...
Job ID: 88443The Senior Clinical Project Manager will provide end-to-end operational leadership for my client's clinical trial(s), ensuring delivery to time, cost, and quality standards. This individual will establish fit-for-purpose clinical operations frameworks, oversee CRO-led execution, and build a high-performing internal team while maintaining inspection readiness at all times.This role is...
Global Study Manager Duration - 12 months (interim) Location - Remote Inside IR35 Rate - £500.00 (Umbrella) or £402.00 (PAYE) per day The Global Study Manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance. The exact accountabilities will differ depending on the exact nature of the clinical program, so a high degree of flexibility is...
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner. Key Responsibilities - Manage clinical supply strategies within clinical studies whilst ensuring these delivered in a timely and cost-efficient manner
The Scientist for Clinical Trials - Oncology - Thoracic (Sr. Manager)( non-MD ) is responsible for providing support of scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio .Job ResponsibilitiesClinical development professional maintaining current scientific and clinical...
Senior Clinical Research Associate (Oncology)Working embedded with a leading global oncology-focused biopharmaceutical companyWe are partnering with a top-tier global biopharmaceutical organisation to support a growing oncology portfolio and are seeking an experienced Clinical Research Associate to join the team in an advanced, hands-on clinical role.This position offers the opportunity to work...
Global Study ManagerDuration - 12 months (interim)Location - RemoteInside IR35Rate - £500.00 (Umbrella) or £402.00 (PAYE) per dayThe Global Study Manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance. The exact accountabilities will differ depending on the exact nature of the clinical program, so a high degree of flexibility is...
The Scientist for Clinical Trials - Oncology - Thoracic (Sr. Manager)( non-MD ) is responsible for providing support of scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio . Job Responsibilities Clinical development professional maintaining current scientific and clinical knowledge in...
Clinical Trial Manager – UK | Advanced Clinical (FSP Model) Oncology focused Advanced Clinical is seeking an experienced Clinical Trial Manager to join our UK-based Functional Service Provider (FSP) team. This role will support global clinical studies and requires strong operational, vendor management, and monitoring oversight experience. Preparing key study documents, including Monitoring...
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.
Global Study Manager Duration - 12 months (interim) Location - Remote Inside IR35 Rate - £500.00 (Umbrella) or £402.00 (PAYE) per day The Global Study Manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance. The exact accountabilities will differ depending on the exact nature of the clinical program, so a high degree of flexibility is required....
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.