Clinical Trials Management Jobs in Cambridge

The Director Global Medical Affairs will function as medical lead for dedicated projects driving the launch of Key Brand in Nephrology. This role focuses on building and executing the medical plan for launch activities and supporting cross-functional launch preparation ex-USA while adhering to the h...

As a Principal Medical Writer you will provide communication expertise and lead a strategy-driven approach to authoring of key clinical and regulatory documents and regulatory submissions to ensure clarity credibility and consistency of clinical information throughout submission packages and clinica...

Job Purpose The Manager of Clinical Data Management is responsible for the oversight and management of data management activities to ensure high quality data collection tools database design and oversight of data management activities of MoonLake sponsored clinical trials.Majo...

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...

Job Purpose As a Clinical Trial Administrator you will provide administrative support and maintain essential clinical documentation for MoonLake sponsored clinical studies.Key Accountabilities:Provide document management and filing support for MoonLake Clinical Development Pro...

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 DescriptionJoin Us as a Medical Writer - Make an Impact at the Forefront of InnovationThe Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal a...

DescriptionPlease note we have a separate job advert for candidates interested in joining our Value and Access or Evidence Development teams which you can find here: Costello Medical - Current Openings. Please apply for one role at a time because assessment processes differ. Role Summary Responsibil...

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 CategorySafetyJob 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 collabo...

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...

As a Data Solutions Lead Senior Manager you will oversee a diverse team of Data Collection owners across four sites in Europe. Your teams will be responsible for end to end execution of high impact data collections that drive improvement of General Intelligence models. Youll drive business value by...

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...

DescriptionRole Summary Responsibilities: In this role you will gain hands-on experience in critically appraising and interpreting complex statistics planning and analysing clinical trial data and synthesising evidence with one-to-one training and mentoring from our experienced Statistics team Salar...

DescriptionRole Summary Responsibilities: In this role you will gain hands-on experience in critically appraising and interpreting complex statistics planning and analysing clinical trial data and synthesising evidence with one-to-one training and mentoring from our experienced Statistics team Salar...

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...