Kathryn Taylor

RWE Scientist - United Kingdom - 6 Month ContractOur client is a global biopharmaceutical company manufacturing plasma-derived, and recombination therapeutic products, who in turn deliver high-quality medicines that treat people with rare and serious diseases, and we are now searching on an exclusive basis with the client to appoint a Real World Evidence Scientist to join their busy and rewarding team on a contractual basis for a period of 6 months.What you'll do: Lead the design, execution, and analysis of real-world and observational research studies, ensuring methodological rigor and fit-for-purpose designsManage in-flight Phase IV and post-approval epidemiologic studies; oversee vendors/CROs to ensure quality and timely deliveryConduct and oversee retrospective analyses using large real-world data sources (e.g., claims, EHRs, registries)Contribute to the development of RWE plans and lead feasibility assessments with a focus on Europe (NITAG/regulatory awareness beneficial) What you'll need: Advanced degree (MD, PhD, or MS) in Epidemiology, Biostatistics, Public Health, or a closely related fieldProgressive epidemiology or real-world evidence experienceExtensive experience within Pharma or BiotechAbility to work independently and assume ownership of ongoing work with minimal ramp-up If this role is of interest, please apply now!#LI-KT1

Senior Process Quality Excellence Specialist - UK, West London - 12 Month ContractWe are looking for an experienced Senior Process Quality Excellence Specialist for a fantastic 12 month contract based in West London. You will be working with our client who are a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease. This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first. What you’ll do: Manage Regulatory Intelligence (RIN) requirements for GCSO and coordinate with relevant SMEs.Review regulations and assign SMEs based on topic expertise.Serve as point of contact to ensure CROs assess all applicable regulatory and country‑specific requirements.Act as Audit Host, coordinating internal audits and supporting SMEs during auditor interactions.Support post‑audit activities, including responses to findings, CAPAs, and audit closure. What you’ll  need: Ideal candidates have experience as a Clinical Trial Associate or Clinical Trial Specialist.Exposure to audits is highly desirable.Regulatory Intelligence experience is a strong advantage.A blend of clinical operations background and quality/regulatory awareness is preferred.Overall, candidates should bring a mix of clinical trial support, audit familiarity, and regulatory insight. If this role is of interest to you, please apply now! #LI-KT1

Information Scientist (Content Analysis) - UK, Slough / Remote - 12 Month ContractWe are looking for an experienced Information Scientist for a fantastic 12 month contract based in Slough. You will be working with our client who are a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease. This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first. What you’ll do: Design and implement workflows for literature mining, summarization, and trend analysis using AI/NLP tools.Develop and maintain external information endpoints, ensuring FAIR principles (Findable, Accessible, Interoperable, Reusable) and interoperability.Apply machine learning and large language models (LLMs) to enhance information retrieval and automate content classification.Support pharmaceutical R&D processes. What you’ll  need: Experience or interest in NLP and LLM applications (transformers, Retrieval-Augmented Generation, prompt engineering)Familiarity with data visualisation and scientific communication toolsKnowledge graph and ontology managementPython and AI frameworks for text analytics If this role is of interest to you, please apply now! #LI-KT1

Supply Planner - UK, Surrey - 6 Month ContractOur client, a speciality pharmaceutical company based in the South of the UK are looking for a Supply Planner. Experts in their field they have a focus on the central nervous systems, gastroenterology, ophthalmology and rare diseases identifying difficult to manufacture therapeutic products and working with trusted partners to get them to the market. What you'll do:  Plan and coordinate the replenishments of FGs to Distribution Centre and 3rd party partners- contact point for DistributorsKeep Commercial up to date of all stock positions so that focused sales campaigns can be delivered when needed.Monitor available stock levels meticulously to minimize write-offs due to expiration and prevent destruction by initiating redistribution activities when feasible.Manage supplier relationship with CMOs to establish a strong partnership What you'll need: A certification in supply chain management or related field can be helpful in this roleSignificant experience in a pharmaceutical industry and / or in FMCGExperience of forecasts, planning and inventory managementProven experience of having an analytical / numerical /data driven approach If this role is of interest, please apply now!#LI-KT1

Medical Advisor - UK, London - 12 Month ContractOur client is based in London and supporting manufacture drug substances, reinforcing its commitment to women’s health and fertility care. We are looking for a Medical Advisor to join their team on a 12 month contract to help with the production of high-quality treatments to grow as a leading women’s healthcare company. What you'll do: Ensures execution of agreed medical tactics and leverage best practicesCommunicate scientific therapy needs credibly, appropriately, and effectively across a variety of internal and external stakeholders at all levels.Build trust with the external scientific community via peer-to-peer scientific exchange, research and educational collaborations, interactions with scientific societies and health organisations, publications, etc.Provide therapeutic/functional training to assigned teams and affiliate functions.  What you'll need: MD, PhD in health sciences, Pharm D or equivalent.Strong experience as Medical Advisor or equivalentExperience of relevant pharmaceutical industry guidelines (ABPI Code of Practice), regulatory / reimbursement framework and clinical research guidelines.Scientific knowledge and experience within neurology/migraine is preferred.Strategic thinking If this role is of interest, please apply now! #LI-KT1

QA Clinical Specialist - UK, Slough - 12 Month ContractWe are looking for an experienced QA Clinical Specialist for a fantastic 12 month contract based in Slough. You will be working with our client who are a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease. This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first. What you'll do: Support the HPQE in GCSO quality and compliance infrastructure development; assist with creation/revision of appropriate quality and compliance policies, Standard Operating Procedures (SOPs), processes, and best practices as needed.Lead and drive GCSO Inspection Readiness Activities across all GCSO functions working closely with the relevant inspection team(s).Participate in Audit and Inspection planning with Global Quality.Represent or ensure GCSO representation including preparation during audits/inspections (on-site at UCB by internal and external parties). What you'll need: Extensive pharmaceutical experience, preferably in a global Quality Assurance or a Clinical Development setting.In depth experience of GCP and GVP, including hands on experience in global GCP audits and/or inspections.Extensive experience in SOP writing essential. If this role is of interest to you, please apply now! #LI-KT1

PV Officer - UK, Hertfordshire - Permanent ContractOur client manufactures and sells its own forms of various generic and legacy medicines, using Prescription Only Medicines (POMs). They are looking for a PV Officer to work on their project based in Hertfordshire, on a fixed term contract. What you'll do: Responsible for continuing development and maintenance of the AE reporting processes and system.Responding to Medical Information (MI) enquiriesExecute literature searches to identify key product articlesCreation and collation of aggregate reports (PSURs, RMPs, Renewals etc,) What you'll need:  Relevant experience working in the pharmaceutical industry is preferred.A willingness to learn and grow with the team is essentialBSc or equivalent Life Sciences DegreeExcellent communication skills, written and oral and fluent in English Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-KT1

Quality Assurance Officer - UK, Hertfordshire - 12 Month ContractOur client manufactures and sells its own forms of various generic and legacy medicines, using Prescription Only Medicines (POMs). They are looking for a Quality Assurance Officer to work on their project based in Hertfordshire, on a fixed term contract. What you'll do: Supporting the QA manager (RP/RPi) with the maintenance and effectiveness of the Quality management system.Ensure Deviations, CAPAs and change controls for which you are the owner are progressed in a compliant and timely mannerEnsure customer complaints are satisfactorily investigated and communicatedUnderstand, and accurately follow internal quality procedures and GMDP in accordance with guidelines and legislations. What you'll need: Experience having worked in an QA capacity Right to work in the UKUnderstanding of quality management systemsExperienced in management of Deviations, Complaints, Change controls and CAPAAbility to review documents and generate PQR Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-KT1

PV Associate - UK, Hertforshire - Permanent ContractOur client manufactures and sells its own forms of various generic and legacy medicines, using Prescription Only Medicines (POMs). They are looking for a PV Associate to work on their project based in Hertfordshire, on a permanent contract. What you'll do: Processing serious and non-serious adverse events, spontaneously reported adverse reactions and/or other medically related project information such as adverse events of special interest and clinical endpoints.Responding to Medical Information (MI) enquiries in a timely fashion and within the timelines as documented in internal proceduresExecute literature searches to identify key product articles for signal detection reports, drug safety relevance etc What you'll need: Qualified up to BSc or equivalent life science degreeMust have valid right to work in the United KingdomDesirable to have experience having worked in medical information and/or pharmacovigilance preferredExcellent communication skills, written and oral and fluent in English Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-KT1