Kathryn Taylor

Medical Advisor - UK, London - 12 Month ContractOur client is based in Central Netherlands and manufacture drug substances for fertility products, 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