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:
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
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...
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...
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...
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...
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.
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...
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
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,...
A leading pharmaceuticals organisation is seeking a Senior Legal Counsel to join their organisation. The organisation is a leader in providing specialist products and technologies to healthcare markets globally. About the role:As Senior Legal Counsel you will be responsible for providing legal support for the clinical trial business which operates across Europe and the US and will act as business...
Job Title: Clinical Research Associate (CRA)Location: Remote (UK Residency)Contract Period: PermanentRequirements: (UK Right to Work)Company Overview:Apsida Life Science has partnered with a leading global Clinical Research Organization (CRO) renowned for its scientifically driven programs. They specialise in managing complex Phase I–IV trials across diverse therapeutic areas for innovative...
You will support a diverse range of clinical studies/trials involving patients and healthy volunteers, undertaking drug development programmes in a variety of therapeutic fields, including respiratory, dermatology, cardiovascular, endocrinology, and inflammatory disorders. Key responsibilities:To provide medical care and oversight of clinical trial participants.
A leading clinical research organization in London is seeking a Psychiatrist Medical Director to provide medical and strategic leadership for clinical trials. The role involves overseeing medical management, contributing to regulatory documents, and ensuring safety in trials. Candidates should possess an M.D. degree and experience in clinical trial research is preferred. The position offers a...
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...
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...
A global clinical research organization is seeking a Director, Feasibility, to lead within their Proposals and Feasibility team. The role entails evaluating new clinical trial opportunities, collaborating with various stakeholders, and leveraging expertise in clinical trial management. Candidates should have a Bachelor's degree and extensive experience in the industry. This position offers a...