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As a highly driven Senior Scientist, you will be supporting the R&D Team in the development and optimisation of novel diagnostic assays.
You will be instrumental in delivery of analytical activities across a portfolio of new respiratory products, successfully leading projects as they progress into clinical studies and through to commercialisation!
As a Senior Manager (Analytical Team) you will lead on delivery of all analytical activities taking new products through to clinical studies and subsequently commercialisation. The main focus of research is respiratory treatments.
The client are a developing biotech undergoing expansion, with the aim to support in development of novel t-cell therapies.
You will utilise existing knowledge and a variety of research methods relating to cell line engineering, molecular techniques and screening assays to support development of novel t-cell therapies.
As a Study Operations Manager you will be responsible for coordinating and overseeing delivery of a number of clinical studies from an organisational point of view. You will directly manage a team of Senior Scientists to deliver.
As a Principal Scientist with focus on analytical chemistry you will provide SME support with analytical testing, scientific consulting and regulatory support to help key customers advance key products into the market!
You will be responsible for development of new analytical methods to support a number of client projects. You will support in development and troubleshooting activities to progress projects, whilst working in line with regulatory standards.
As a QA Auditor within the QA team you will plan and conduct audits of processes, systems, facilities, studies and documents to ensure compliance with GCP. You will play a vital role in ensuring general compliance and effectiveness of the CRO.
You will conduct relevant surveys and provide specialist advice from an Ecological point of view, helping embed the approach from the very beginning of new projects.
As a Senior Scientist you will be involved with extraction and analysis of a range of samples to screen for compounds of interest, such as drug compounds. You will also support with method development activities and supervising / training of scientists.
As a Principal Scientist you will be an SME in your area supporting, advising and overseeing a number of specified clinical studies. You will perform a key role in the development of scientific operational staff.
I'm currently looking for a Quality Coordinator based in Gloucestershire, this position requires someone with experience in a QA/QC position within labs, and experience working to ISO17025.
Exciting opportunity for an experienced regulatory lawyer to join a global animal health company on their general legal team, working from Liverpool. A competitive salary is on offer.
Working in the Project Management team as project owner, assisting with technical and commercial aspects. Running projects in a controlled and timely manner, utilising project management methodologies and planning in accordance with multi-site processes.
Research Assistant to contribute to the development of hydrogel drug delivery systems for the oral administration of small molecules and biologics.
Maintaining a focus on the value of patient-centric outcomes whilst ensuring that clinical programs have a innovative PRO/COA Strategy. Defining and overseeing the execution of strategies and guiding the development and validation of instruments in clinical trials and studies.
To effectively aid in ensuring validation studies and activities are planned and executed in line with defined external and internal standards. The main focus of the role will be process validation, equipment qualification and cleaning validation.
Working with the editing team to help manage and maintain professional scientific standards.As part of the publishing team, you will act as liaison between all internal and external parties.
Responsible for providing technical support to the Toxicology team working alongside the Head of R&D, Method Development & Quality. Proficient, to a legally defensible standard, in techniques such as immunoassay, LLE, SLE, and liquid chromatography-mass spectrometry.
You will provide technical expertise and project management across bioanalytical activities, including oversight of outsourced bioanalysis at CROs for both clinical and pre-clinical drug development.
As a Senior Research Scientist in the clinical trial space, you will be leading the analytical stage of clinical trials and acting as a technical Subject Matter Expert (SME) in the scientific discipline.
As a Clinical Research Associate, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs and medical devices experts to identify, select, initiate and close-out investigational sites for pre and post market studies, ensuring adherence to applicable regulations and principles of ICH-GCP.
As a Senior Proposal Manager you will be responsible for managing all aspects of proposals, monitoring and overseeing the scope of work and budgeting process to generate accurate and timely proposals.
Manage and coordinate all laboratory operations, including sample processing, data analysis, and quality control procedures. Oversee the allocation of resources, ensuring optimal utilization of equipment, supplies, and personnel.
As an SDS Specialist / Hazard Comms professional you will primarily focus on working within the EU market to provide technical scientific input into SDS generation / updates.
The purpose of this role is to make sure that the labelling is updated and compliant and meets the necessary trademark deadlines.
Leading development and validation activities with predominant focus on LCMS / triple quad MS, designing and developing quantitative bioanalytical methods in support of PK and PD projects
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