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 -
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 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
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
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: 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
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 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
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
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
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