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 play a pivotal role in leading the design, analysis, and integration of cutting-edge methodologies across AI, biostatistics, and clinical epidemiology, with a focus on transforming health outcomes through advanced digital trial frameworks.
You will provide leadership within the research team, collaborate cross-functionally, and maintain the highest standards of participant safety, protocol compliance, and data integrity in complex and sensitive research environments. Key responsibilities include:
You will provide leadership within the research team, collaborate cross-functionally, and maintain the highest standards of participant safety, protocol compliance, and data integrity in complex and sensitive research environments. Key responsibilities include:
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...
You will have a lower than average number of protocols, setting you up to be a protocol expert.
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
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
A leading AI research firm is looking for a Principal Clinical Scientist to help design and review clinical trial protocols and ensure clinical data complies with regulatory standards. Ideal candidates will have senior-level experience in clinical trials, deep expertise with regulatory agencies like the FDA, and a strong background in biostatistics. The role offers competitive hourly pay between...
CTS Project ExecutiveCompany & Role DescriptionFounded in 2002, Tanner Pharma Group is a specialty service provider in the biopharmaceutical industry focused on improving patient access to medicines on a global basis. Tanner Pharma offers its biopharmaceutical partners a portfolio of four distinct service offerings that span the product lifecycle from clinical development to commercialization....
Position: Clinical Supply Operations TechnicianLocation: Moreton, DorsetClient: PharmaceuticalType: 12 months contractMain ResponsibilitiesCarry out clinical trial packaging operations, including start-up, execution, cleaning, and completion, in line with SOPs and GMP.Perform primary packaging, labelling, and assembly of clinical trial supplies using manual and automated equipment.Monitor...
A leading clinical research organization in Greater London is seeking a Dermatologist - Medical Director to provide strategic leadership for clinical trials. Responsibilities include medical management, contributing to study reports, and coordinating with various teams. Preferred qualifications include an M.D. degree and experience in clinical research. The position offers hybrid work flexibility...
A leading clinical research organization is seeking an experienced Clinical Director to lead the Early Phase unit in Manchester. This role combines strategic leadership in clinical operations, requiring at least 10 years of experience in clinical trials and a strong background in Phase I drug development. The successful candidate will manage local teams, ensure project excellence, and act as a...
You will manage over 30 staff, ensuring the safe delivery of clinical trial medicines and contributing to service development. The ideal candidate will have significant experience in clinical research and hospital pharmacy. The role offers a flexible working environment with opportunities for career development, located in Southampton, a city known for its accessibility and natural beauty.
Job Title: Senior Research Nurse – Respiratory and COPD studiesSalary: £50000 per annum (dependent on experience)Location: Central LondonAre you an experienced research nurse with a passion for advancing care in respiratory health? We are recruiting on behalf of a prestigious private hospital in Central London for a Senior Research Nurse to join a leading clinical trials team focused on COPD and...
Clinical trials are high stakes, demanding high standards. Veramed sets this standard by bringing together the sharpest minds in data management, biostatistics and programming, with cutting-edge technology and proven processes.Our globally connected, caring team delivers quality, precision and collaboration, earning trust through consistency and integrity. From rapid-fire project work to...
CRO Solutions ® , an IQVIA business is recruiting for a 12-month maternity cover CRA I position to join an existing team of established CRAs, working on a range of clinical trials. The position will be a hybrid role of office based (in our premises in Salford, Manchester) and work from home when not monitoring at study sites. Clinical trial experience is essential for this role, which would suit...
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...
You will work closely with the clinical trial team to ensure activities are conducted in accordance with GCP, SOPs, and regulatory standards. Key Responsibilities - Support activities for Phase 1–4 studies from feasibility and start-up through close-out
You will be part of a collaborative environment where your contributions will have an impact.
A clinical research organization is seeking a Pediatric / Neuromuscular Neurologist Medical Director to provide strategic leadership for clinical trials. The role involves managing medical expertise, safety assessments, and coordinating new clinical project developments. The ideal candidate will have an M.D. degree and clinical trial experience. This position offers hybrid work flexibility,...