7 jobs found in Barnet

Clinical Project Associate 12 month Contract start date ASAP Job Purpose The Project Associate (PA) supports the planning and execution of multiple clinical development initiatives. Working closely with Clinical Development colleagues and cross-functional stakeholders, the PA drives operational efficiency and contributes to successful project delivery. The role ensures project activities are well-organized, deadlines are met, and communication flows effectively. Major Activities * Project Planning, Coordination and Execution: Develop and maintain detailed project timelines, and contribute to content of key deliverables. Ensure all aspects of the project are organized and tracked effectively. Monitor completion status of deliverables, flag issues and opportunities, and escalate as needed. Ensure team is working in alignment with project objectives. Maintain project dashboards and support reporting for governance reviews. * Documentation Management: Maintain and manage...

Talentmark are recruiting for a Senior Regulatory Specialist to join a global pharmaceutical company on a contract basis for 12 months. Salary: £24.50 ph PAYE Senior Regulatory Specialist Role: Lead the development and execution of regulatory strategies in the UK and Ireland Be the local regulatory contact for MHRA and HPRA on assigned products Lead post-approval product information management Drive departmental readiness for audits, inspections, and procedural compliance activities Lead post-approval product information management Your Background: Hold a degree in a relevant scientific subject or have equivalent working experience  Some work experience in a regulatory affairs role in the pharmaceutical industry Knowledge of EU, UK and Irish regulatory processes, GxP and quality systems Experience with regulatory information management (RIM) systems such as Veeva Vault or similar Strategic thinker with strong analytical, problem-solving, and decision-making skills Company:...

A leading biopharmaceutical company is looking for a motivated and collaborative Senior Scientist to join its Preclinical Research team. This is an opportunity to play a key role in advancing translational in vitro models, including organoids, organ-on-chip systems, and cutting-edge microphysiological platforms. You’ll contribute across a diverse pipeline of discovery and development programmes, helping to accelerate therapeutic candidates through preclinical evaluation. Experience in building disease-relevant in vitro models, particularly within autoimmune or inflammatory disease areas, would be highly valuable. Key Responsibilities * Design, develop and optimise organoid-based disease models aligned to immunology and inflammation research e.g. liver, lung, gut * Develop and execute in vitro assays using advanced single- and multi-organ-on-chip platforms * Perform and interpret a range of analytical techniques, including FACS, MSD, ELISA and qPCR * Troubleshoot and...

Job title: Scientist (QC Product Testing and Stability) Location: Slough Contract Length: 12 months Working Hours: 37.5 hours/week Pay: 17.96ph About the Role The role is predominantly lab based for the execution analytical testing e.g. HPLC (size exclusion, ion exchange etc.), electrophoresis (e.g. CE SDS, icIEF), spectrophotometry and general characteristic analysis (e.g. visual appearance, pH, Osmolality) for the purpose of assessing the quality and stability of therapeutic proteins. All work is expected to be carried out in a safe and compliant manner in accordance with local EHS policies and cGMP guidelines. In addition, some time will be spent technically reviewing other analysts assays, writing stability study protocols and data summary reports, SOP updates, and assisting with quality records. Key Responsibilities Performs experimental work independently in accordance with SOPs and study protocols on a variety of sample types Performs work in a safe, compliant manner,...

Your new company You'll be joining a global biopharma company who are expanding their research teams to focus on advancing preclinical discovery through innovative, translational in-vitro technologies, such as organoid culture. You'll work in a highly collaborative environment supporting immunology and inflammation programs across early discovery and development. Your new role As a senior scientist in the R&D team you'll be working alongside an experienced team, carrying out complex in-vitro modelling for drug discovery and development programmes. You will play a key role in developing and applying advanced translational systems to support preclinical evaluation of therapeutic candidates. This is initially a 12 month contract that has the potential to extend and is a lab based role. Key duties include: Designing, developing, and optimising organoid‑based disease models, particularly for immunology and inflammation Implementing and refining complex in vitro assays using...

Locum Pharmacist Required – GP Surgery Start: ASAP Duration: 12 weeks Location: Slough Working Hours: 9:00am – 5:00pm Days: Monday - Friday We are currently seeking a qualified and experienced Pharmacist to join a busy GP surgery on a temporary basis. Role Responsibilities: * Medication reviews and patient consultations * Supporting GPs with prescribing queries * Managing repeat prescriptions * Ensuring safe and effective use of medicines Key Requirements: * Registered GPHC Pharmacist with relevant qualifications * Previous experience working within a GP surgery or primary care setting * Proficient in using EMIS Health clinical system * Strong clinical knowledge and patient-focused approach * Excellent communication and organisational skills This is a fantastic opportunity to work within a supportive healthcare team and make a real difference in patient care

Job title: R&D Scientist Location: Slough Contract Length: 12 months Working Hours: 37.5 hours/week Pay Rate: £17.96/hour About the Role We are currently looking for a Scientist to join our Bioprocess Analytics and Automation group within R&D Protein and Process Analytics. This team is responsible for delivering high-value technical innovation, both via specialist analytical projects and as part of wider collaborative project teams. As a Scientist, you will be responsible for planning and execution of scientific/ experimental work for target projects, including elements of laboratory work, scientific writing and review, testing of new technologies, method development and optimization. This position requires experience in analytical separation and characterization of biotherapeutics proteins, and with analysis of relevant protein CQAs/ PTMs, as charge/ size variant analysis, purity and glycosylation profile. Key Responsibilities: Planning and execution of scientific...