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.
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 NIS P&D Project Management, Associate Director role involves developing and delivering Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams to ensure accurate and aligned project schedules. Key responsibilities include maintaining data quality in Planisware, forecasting costs, and managing risks.
The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality NIS Project Plans, managing resources, and collaborating with various functional teams to ensure alignment with R&D and marketed product portfolios. The role involves maintaining accurate project schedules, forecasting costs, and ensuring data quality in Planisware.
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.
Were recruiting for a growing, globally active medical device company seeking a Junior Clinical Project Manager to support clinical development and clinical affairs activities across EMEA.A strong opportunity for an early-career professional to gain hands-on experience across clinical investigations, investigator-initiated...
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 clinical safety strategy for drug projects and products, ensuring the safety and risk management of AstraZeneca's pharmaceuticals. You will work on evaluating adverse events, communicating safety data, and contributing to regulatory submissions, all while collaborating with a global team of experts.
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.
