Biotechnology Research Jobs in UK
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Senior Project Manager Regulatory Governance Readi...
Together
Were looking for an experienced Senior Project Manager to lead high-impact strategic initiatives. You will be focusing on our new regulatory change portfolio and with support from Leadership and the wider team be a key voice in the setup and definition of the Portfolio. Reporting to the Head of Deli...
Regulatory Affairs Associate (12- Month Secondment...
Catalent
Regulatory Affairs Associate 12-month SecondmentLocation: Swindon UKPosition summary; Monday Friday 37.5 per week (3 days onsite 2 days remote)As a Regulatory Associate you will support the delivery of highquality regulatory projects ensuring all activities meet agreed timelines comply with applica...
Associateprincipal Medical Writer
Trilogy Writing And Consulting
Senior/Principal Medical Writer Remote/Hybrid/In Office - UKTrilogy Writing & Consulting AnIndegeneCompanyis currently looking to hire Senior/PrincipalMedical Writers (f/w/d) to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical indus...
Snr Assoc Legal Director Residential Development
Errington Legal
Seeking an experienced Residential Development solicitor to join a leading UK law firmSenior Associate/Legal Director - Residential Development(Sector focused) - East Anglia or London with hybrid workingClientAn expanding team within a forward-thinking full service leading UK law firm with excellent...
Medical Writer
M3usa
We are looking for creative resourceful and enthusiastic writers to join our team. The Medical Writing team at M3 (EU) is responsible for producing a wide variety of content for including promotional material conference highlights videos case studies education modules and more for a range of client...
Associate Medical Writer
M3usa
We are looking for creative resourceful and enthusiastic writers to join our team. The Medical Writing team at M3 is responsible for producing a wide variety of content primarily for the UKs largest professional network of doctors but additionally for a range of other media. Content produced includ...
Sr Associate Regulatory Affairs Cmc (x2)
Amgen
Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATIONIf you feel like youre part of something bigger its because you are. At Amgen our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global col...
Medical Writer Iii, Ai-assisted Operations
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Senior External Affairs Manager
Iosh
DescriptionJob Title: Senior ExternalAffairs ManagerSalary: 45000- 50000 (based on experience) Hours per week: 35Location: At IOSH we embrace hybrid working because we believe its the key to achieving work-life balance strategic success and fostering our collaborative culture. Youll be required to w...
Medical Writer Iii, Ai-assisted Operations
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Manager, Regulatory Ops- Submission Management
Gilead Sciences
At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...
Fsp Medical Writer (mfd)
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionMedical Writer (EMEA) (FSP; Remote)At Thermo Fisher Scientific you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to...
Channel Manager Europe
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make...
Compliance Analyst Regulatory Affairs
The Vanguard Group
The roleAs a Compliance Analyst youll be at the heart of our regulatory strategy supporting the Regulatory Affairs team within the Compliance function of the Office of the General Counsel (OGC). This is more than an administrative roleits an opportunity to contribute to critical regulatory engagemen...
Senior Medical Writer
Havas
Agency :Havas LynxJob Description :One of the priorities for this role is that you must have prior experience in a creative healthcare comms (i.e. advertising/marketing) agency across promotional materials and medical affairs. Are you passionate about creating advertising that not only informs but a...
Analystmedical Writer Internship 2026
Costello Medical
Description Role Summary Responsibilities: You will have the opportunity to gain hands-on experience with a variety of projects typically working on two to three at any one time and likely across two different teams for the duration of your internship Salary: A pro-rated salary of 25800 per annum ou...
International Regulatory Affairs Director
Astrazeneca
The International Regulatory Affairs Director (IRAD)is responsible fordeveloping and implementing the international regulatory strategy for a group of products. This role ensures that the strategy is designed to achieve rapid approval withadvantageouslabelling aligning with the product properties an...
(senior) Director Clinical Development
Sobi
Including but not limited to the following:Shape and develop the clinical development plans while adhering to the highest scientific and ethical standardsDesign conduct and report Sobi-sponsored studies in close collaboration with the rest of the clinical development team the clinical study teams re...
Fsp Principal Medical Writer (emea)
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionPrincipal Medical Writer (EMEA) (FSP; Remote)At Thermo Fisher Scientific you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our cu...