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
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 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.
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...
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...
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...
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,...
You will be instrumental in ensuring protocol compliance, accurate data collection and a positive patient experience throughout the study lifecycle. Key ResponsibilitiesOversee clinical trial nursing activities from initiation to close‑out in accordance with ICH/GCP guidelines.
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.
Business Support ManagerReading6-month contract£510.00 per day UmbDescriptionOur client is a Global Pharmacutical and biotechnology company and they are seeking a Business Support Manager to join our global clinical operations team. This role will focus on enabling efficient study start-up, monitoring, clinical trial management, and electronic Trial Master File activities, ensuring maximum...
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....
Project Manager (Clinical Systems) UK - remote About the ClientOur client is a global leader in clinical trial technology, providing advanced software solutions that accelerate the development of life-saving medicines and medical devices. They maintain one of the world’s largest collections of clinical trial data, supporting the majority of top-selling pharmaceutical products through innovative...
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...
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...
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.
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...
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...
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: