Clinical Development Jobs in Cambridge

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Medical Writer - Make an Impact at the Forefront of InnovationThe Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts...

Career CategoryClinicalJob DescriptionHOW MIGHT YOU DEFY IMAGINATIONAt Amgen every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared missionto serve patientshas driven our status as one of the worlds preeminent biotechnology companies reaching over 1...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionPrincipal Medical WriterAt 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 worl...

The Scientist for Clinical Trials - Oncology - Thoracic (Sr. Manager) (non-MD) is responsible for providing support of scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.Job Responsibilitie...

The Associate Director Medical Affairs Tryngolza sits within the global Tryngolza medical affairs and clinical development (MACD) team and is responsible for supporting the execution of the global medical plan for the assigned product in collaboration with the rest of the global medical team as well...

DescriptionSenior Quantum Error Correction ResearcherCambridge UK Full-time PermanentHybrid72000to 140000(DOE) Bonus BenefitsThe salary range for this role is broad as weare able toconsider varying levels of offer made will carefullytake into accountlevel of experience (including relevant industr...

The Global Product Safety Science Lead (GPSSL) is responsible to strategically lead the Safety Science activities for assigned Sobi products. The GPSSL leads the safety science engagement throughout the product lifecycle including the development and maintenance of the clinical safety profile of the...

The Global Product Safety Scientist (GPSS) is responsible for providing safety scientific expertise and works with the Global Product Safety Science Lead (GPSSL) to develop and implement the Safety Science strategy for assigned Sobi products.  The GPSS works collaboratively together with the GPSSL a...

Job Title: SeniorScientistIntegrated Bioanalysis ImmunoassaySpecialist(levelD)Location: Multiple locations (Sweden&UK)AboutDiscovery BioanalysisDiscovery Bioanalysis (DxBA) is a global department within Integrated Bioanalysis Clinical Pharmacology & Safety Sciences supporting AstraZenecas portfolio...

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...

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...