Clinical Development Jobs in Cambridge

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThe Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. The role involves collaborating with internal and exte...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll 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 make the world healthier cleaner and...

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...

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...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionPosition Overview:We are seeking a highly skilled and experienced professional in Europe to oversee clinical pharmacology deliverables and serve as an ESA Subject Matter Expert (SME). The ideal candidate will have a strong b...

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...

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...

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...

The Scientist for Clinical Trials - Late Stage (non-MD Director) is responsible for scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio. The successful candidate may have managerial respon...

The Head of (Executive Director) International CMC Regulatory Affairsreports to the VP International Regulatory Affairs and is accountable for leading a team of Regulatory professionals (7-10 direct reports at Director level and 30-40 indirect reports) responsible for strategy delivery and execution...

The Head of (Executive Director) International CMC Regulatory Affairsreports to the VP International Regulatory Affairs and is accountable for leading a team of Regulatory professionals (7-10 direct reports at Director level and 30-40 indirect reports) responsible for strategy delivery and execution...

The Head of (Executive Director) International CMC Regulatory Affairsreports to the VP International Regulatory Affairs and is accountable for leading a team of Regulatory professionals (7-10 direct reports at Director level and 30-40 indirect reports) responsible for strategy delivery and execution...

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...

Senior Scientist in Translational Pathology OncologyWe are seeking a Senior Scientist to join the Translational Pathology group in Oncology R&D Translational Medicine department where you will be at the forefront of the evolution of translational science for a global oncology group in AstraZeneca!Yo...

Senior Scientist in Translational Pathology OncologyWe are seeking a Senior Scientist to join the Translational Pathology group in Oncology R&D Translational Medicine department where you will be at the forefront of the evolution of translational science for a global oncology group in AstraZeneca!Yo...

The Senior Manager Regulatory Affairs CMC will be responsible for the development execution and tracking of CMC regulatory activities for assigned BicycleTx programs or projects.You will be responsible for supporting the development of CMC regulatory strategy and processes for their assigned Bicycle...

Job Title: Pathology Manager in Translational Pathology OncologyLocation: Cambridge Salary: CompetitiveIntroduction to role:Are you ready to make a difference at AstraZeneca We are seeking a Pathology and Sample Manager to join our Translational Pathology group within the Oncology R&D Cancer Biomark...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThermo Fisher Scientific Clinical Research Group is a leading CRO. The Clinical Research Group (CRG) has again been recognized for excellence in the 2025 CRO Leadership Awards. This is the 14th consecutive year the business...