10 pharmaceutical jobs found in South East

Job title: Senior AnalystLocation: Abingdon, Oxfordshire (on site full time)Contract length: Until 31/04/2025, covering maternity leavePay rate: £35,000 per annum My client is part of a family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. The position of Senior Analyst is within

JOB TITLE: Contract Specialist - BidsLOCATION: Office based - MaidenheadSALARY: £45,000 - £47,000 The Role:Are you ready to take the lead in securing critical business contracts? We're seeking a proactive and detail-oriented Contract Specialist to join our dynamic team at our Maidenhead office. In this role, you'll play a pivotal part in our tender submission process, working closely with Contracts Managers across the country to deliver accurate and timely

Job Title: Medical Safety Analyst DevicesLocation: SittingbournePay Rate: £23-£30 per hourDuration: 12 MonthsResponsibilities:Process consumer complaints related to enteral feeding medical devices in accordance with applicable regulations.Collect, assess, and document medical device complaints and adverse events promptly and compliantly.Conduct follow-up calls with customers to gather additional details on adverse events and complaints.Code complaints usin

Bioanalyst (Research Scientists - Non-Regulated Bioanalysis) x2Location: Slough, UKWorking Hours: 37.5 hours per week, 7.5 hours per dayContract Length: 12 months, possibility of extensionStart Date: ASAPRole Overview: We are currently seeking two experienced Bioanalysts to join our team in Slough, UK, to support non-regulated bioanalysis research projects. The positions are available due to maternity cover and additional resource requirements. The contrac

Biomarker ScientistLocation: Slough, UKDepartment: Biomarker Assay Sciences, Early Clinical Development and Translational Science (ECD&TS)Salary: £20.03 per hourWorking Hours: 37.5 hours per week, 7.5 hours per dayThe Biomarker Assay Sciences group is an integral part of Early Clinical Development and Translational Science (ECD&TS) department, providing strategic support in various areas including pharmacokinetics/pharmacodynamics, DMPK, biomarker analysis

Position: Office Administrator (Support Clinical and Science Support teams)Location: WitneyWorking Days: Mon-FriPay Rate: £26,000 Main Purpose of RoleThe primary objective of this role is to deliver high-quality and efficient data management support to Clinical Affairs, the Science Support Group, and other departments as needed.Main ResponsibilitiesPerform and oversee the upload and verification of data from multiple sources.Monitor the entry and migration

Do you consider yourself to be an organised individual, with great communication skills? Are you able to work effectively to provide procedural reports and updates? If so, we are looking for an individual who would be interested in joining a UK EHS Commercial Manager. You will be responsible for a number of tasks from supporting issues or incidents, conducting reviews and chairing committee meetings.Role details:Title - UK EHS Commercial ManagerLocation -

Are you an experienced Labelling Lead? Do you have pharmaceutical or biotechnology regulatory experience, including regulatory labelling? If so, our Biotechnology client is looking for individuals just like you! The purpose of the Global Labelling group is to drive the core labelling strategy and ensure that labelling documents are of high quality and compliant for the safe and effective use of our clients products for patients and healthcare providers glo

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working