11 jobs found in Ascot

This team plays a key role in advancing both small molecules and biologics from early discovery through to development. As a Senior Scientist, you’ll bring strong scientific expertise and a hands-on approach in the lab, contributing directly to ongoing programmes. The role is centred around experimental delivery, scientific rigour, and collaborative project support. You’ll design, execute, and interpret in vitro studies, generating high-quality data that drives critical project decisions. What You’ll Be Doing * Designing, planning, and executing in vitro studies for target identification, validation, and translational pharmacology * Applying technical expertise in immunology models to ensure robust and relevant experimental design * Testing and validating small molecule and biologic candidates * Establishing, optimising, and validating in vitro systems, including managing outsourced work with CRO partners * Reviewing and interpreting complex datasets to support...

Your new company You'll be joining a global biopharmaceutical organisation driving innovation across a number of disease areas. You'll be part of an experienced team, working in a collaborative research environment supporting the discovery and early development of next‑generation therapeutics. Your new role This is initially a 12 month contract position, based completely in the company's labs. As a Senior Scientist working on in-vitro immunology studies, you will provide scientific leadership and hands‑on support to advance discovery and early development programs. Key responsibilities include: Designing, planning, and carrying out in vitro studies to support target identification, validation, and translational pharmacology Providing hands‑on technical expertise in in-vitro immunology models, ensuring appropriate model selection, scientific rigour, and alignment with project needs Testing and evaluating small molecules and biologics using relevant in-vitro model systems...

Your new company You'll be joining an experienced team in a leading biopharmaceutical organisation focused on advancing innovative antibody and protein therapeutics. You'll be part of a collaborative R&D environment dedicated to developing high‑quality formulations that support all stages of product development. Your new role This is initially a 12 month contract position that has the potential to extend. The role is fully based on site at the company's labs. As a Scientist in antibody formulation development, you will support non‑clinical and clinical programs by developing, analysing, and optimising formulations for monoclonal antibodies and novel therapeutic formats. Key responsibilities include: Performing analytical and formulation experiments to support toxicology and clinical studies Conducting protein/antibody analysis using methods such as HPLC/UPLC, iCE, UV spectroscopy, DLS, CGE, rheology, and sub‑visible particle analysis Supporting pre‑formulation and...

Are you a motivated Clinical Pharmacist looking for a role where you can make a genuine impact on patient care? We’re supporting a leading, well-established healthcare organisation in the search for an exceptional pharmacist to join their clinical pharmacy team. This is a fantastic opportunity to work within a modern, high-performing hospital environment known for delivering outstanding patient outcomes. The Role As a key member of the multidisciplinary team, you will: * Conduct detailed medication reviews for inpatients and outpatients, ensuring safe, effective, and evidence-based use of medicines. * Provide personalised advice to patients on treatment plans, side effects, and adherence. * Review and authorise prescriptions in line with clinical guidelines and regulatory standards. * Promote safe, cost-effective prescribing by supporting compliance with local and national medicines policies. * Contribute to antimicrobial stewardship initiatives and monitor high-risk...

Essential Requirements · A recognised professional qualification in counselling, psychotherapy, psychology or mental health (e.g., BACP, HCPC or UKCP registered). · Minimum 3 years’ post-qualifying experience working with children and young people with complex needs. · Proven experience of delivering 1:1 therapy and/or clinical supervision. · Experience of working within or alongside residential children’s homes or similar trauma-informed services. · A strong understanding of safeguarding, child development, attachment theory, and trauma recovery models. Desirable Skills · Accredited or trained in at least one evidence-based model (e.g., PACE, DBT, EMDR, DDP, or similar). · Training and facilitation experience with mixed-professional groups. · Experience contributing to Ofsted inspections or regulatory frameworks

Housing Needs Research & Data Analyst Initial 3‑Month Contract | Newham | £400 per day (Umbrella) Full-Time (36 hrs/week) | Hybrid | 2-3 Days per Week at Dockside, Newham Monday-Friday, 9AM-5PM Are you a data specialist passionate about using insight to shape public services and combat homelessness? Newham Council is seeking a Housing Needs Research & Data Analyst for a pivotal three‑month contract supporting a data‑driven transformation of Housing Needs services. 🔍 About the Role This role is central to Newham's mission to deliver a robust, intelligence‑led approach to tackling homelessness. You will turn complex datasets into actionable insight, influence strategy, and support senior leaders-including the Mayor, Cabinet, Councillors, Directors, and Chief Executive. Your work will directly shape decisions, performance improvements, and long‑term service design. 📊 What You'll Be Doing Data, Reporting & Business Intelligence Manage and operate key data...

Talentmark is recruiting for a Country Study Start Up Lead to join a company in the Pharmaceutical industry, at their site based in Welwyn Garden City, on a contract basis for 6 months. Salary: Daily: £339 - £376.97 PAYE or £450 - £500 per day Umbrella. Country Study Lead Role: Drive and facilitate efficient study start-up processes to contribute to the delivery of clinical trials to patients. Leading the country strategy for study start-up, driving efficiency, innovation, and collaboration with external stakeholders. Overseeing start-up operations and ensuring timely and efficient site activation and regulatory compliance. Engaging with government and institutional bodies to align on clinical trial policies and practices (e.g., with Ethics Boards, Health Authorities).Your Background: Degree (MD, PhD, MA/MS, BA/BS) in life sciences or equivalent. Postgraduate degree or master’s degree highly desirable Demonstrated experience in clinical trial start-up, regulatory...

Job Advertisement: Senior/Principal Patient-centred Outcomes Research Scientist Location: UK-based office/hybrid (ideally 2 days a week in the office) Contract Type: Fixed Term Contract Contract Length: 9 months Working Pattern: Full Time Hourly Rate: £75 - £90 Are you a passionate and experienced researcher with a focus on patient-centred outcomes? If you thrive in a collaborative environment and are eager to make a significant impact in the pharmaceutical industry, we have the perfect opportunity for you! About the Role: Join our dynamic team as a Senior/Principal Patient-centred Outcomes Research Scientist! In this exciting 9-month contract role, you will play a pivotal part in supporting initiatives. Your expertise will help shape the development and implementation of innovative patient-centred measurement strategies, working closely with a diverse team of PCOR scientists and cross-functional stakeholders. What You Will Do: As a Senior/Principal Patient-centred...

Executive Researcher(Talent Acquisition) Contract: 6 months Working pattern: 2 days per week onsite Join our client, a global leader in healthcare innovation, as an Executive Researcher, where you'll play a pivotal role in identifying and engaging top-tier talent that will help shape the future of medicine. The Opportunity: As an Executive Researcher, you will partner closely with the Executive Search Lead (ESL) to deliver exceptional senior talent that aligns with our mission. This is not just a job; it's an opportunity to be part of a dynamic in-house executive search team dedicated to shaping the future of healthcare. What You'll Do: Talent Intelligence: Utilise your pre-search due diligence to establish expectations and inform the hiring process with competitor market insights and compensation guidance. Research Strategy: Map and pipeline talent through innovative sourcing methods, focusing on diverse senior talent with niche skill sets. Insights Gathering: Leverage your...

Job Title: Laboratory Analyst Vacancy type: 2 Year Fixed Term Contract Area: Hitchin Salary: DOE Key notes: Driving license desirable. Unable to provide sponsorship. SRG is working with a pharmaceutical company near Stevenage and Hitchin that specialises in skin care products. We are looking for an Analyst to join the QC team, providing support with HPLC, GC, and general wet chemistry techniques. This is a fantastic opportunity to get your foot in the door within a pharmaceutical company, covering maternity leave. To be successful in this role, you would need a chemistry/life science degree, and recent experience with HPLC or GC outside of university (e.g work placement). Experience or knowledge working to GMP is highly desirable. Responsibilities include, but are not limited to: Carry out QC or raw materials and finished products using HPLC, GC and wet lab techniques. Conduct equipment maintenance, calibration and solvent disposal, alongside other general lab keeping...

Kinetic PLC are currently seeking a Senior Manager / R&D Programmer to join a busy Pharmaceutical Manufacturing Company, based within the Harlow, Essex area. Duration: 2 years from Start Annual Salary: approx £56,(Apply online only)% Remote - will access systems via your own laptop - VDI connection) 25 Days Annual Leave (pro rata plus Bank Holidays) Position Summary: The Clinical Programming (Contractor) is responsible for providing comprehensive programming support, including managing the timely and accurate execution of programming components of clinical trials. The clinical programming contractor independently manages completed projects that involve global tasks, or cross functional teams The role may require providing inputs to design and analysis, and reporting the results of clinical trials, including programming rules and mocked T/L/G. In addition, providing programming support for publication for our marketed drugs. Essential Duties & Responsibilities:...