Future Tech Jobs
Future Tech Jobs
This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and external stakeholders.
This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to studies. The position also involves mentoring others and contributing to strategic discussions with key stakeholders.
The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.
The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology antibody drug conjugate (ADC) portfolio, focusing on advancing the development of clinical trials from early to late stages. Key responsibilities include protocol development, medical monitoring, safety data review, and collaboration with a multi-disciplinary team of experts to ensure the scientific integrity and timely delivery of clinical trials.
This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.
The Business Insights Manager will analyze data from various sources, including sales and market activity, to develop actionable recommendations that support AstraZeneca’s strategic goals. Key responsibilities include leading market research projects, forecasting, and collaborating with teams in Marketing, Finance, and Market Access, specifically focusing on the Cardio-Renal therapy area.
The Clinical Data Analyst role involves managing and optimizing clinical trial data, collaborating with cross-functional teams, and contributing to the development of data products. Responsibilities include data management, standards validation, pipeline configuration, troubleshooting, and continuous process improvement.
TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...
TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...
As a Project Consultant, you will manage client relationships and oversee the delivery of high-quality projects using Patient Cloud technology. Your responsibilities include managing study portfolios, leading cross-functional teams, and ensuring project milestones are met on time and within budget.
This role involves leading the development and execution of comprehensive translational strategies for Isomorphic Labs' oncology pipeline. You will collaborate with interdisciplinary teams, manage a group of biologists, and ensure the successful transition of AI-designed drugs from preclinical to clinical stages.
Your work will change lives. Including your own.The Impact You’ll MakeWe are seeking an innovative Research Scientist to join our Experimental Immunology team at our new state of the art laboratories in Oxford. In this primarily lab-based role, you will...
The Principal Scientific Programme Manager will lead and support the delivery of specialist External Quality Assessment (EQA) schemes in clinical genomics. This role involves managing timelines, quality, and programme performance, as well as supporting the design and development of new EQA schemes. The position requires strong scientific knowledge, experience in genomics and quality assurance, and the ability to communicate effectively with senior stakeholders.
The Scientific Programme Manager will play a crucial role in international genomics quality assurance, ensuring diagnostic laboratories worldwide produce accurate and reliable genetic test results. Responsibilities include managing EQA schemes, interpreting complex genomic data, and collaborating with senior scientific leaders and stakeholders to maintain high standards and improve diagnostic genomics practices.
Job summaryWe have an exciting opportunity for a Specialist Biomedical Scientist in Clinical Biochemistry/Immunology. The service supports all hospital wards and departments, as well as GPs, clinics, and private hospitals across central and south Buckinghamshire and beyond. The central laboratory...
