Future Tech Jobs
Future Tech Jobs
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 study teams and investigators.
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 study teams and investigators.
The Senior Medical Director will lead clinical research activities for GSK’s oncology portfolio, focusing on developing and executing phase 1-3 clinical trials. They will collaborate with internal and external experts, manage key relationships, and ensure the scientific integrity and timely delivery of clinical trials.
The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing clinical trials from early to late stages. Key responsibilities include protocol development, medical monitoring, safety data review, and collaborating with a multi-disciplinary team of experts to ensure the successful delivery of clinical trials and regulatory approvals.
The RoleJoining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...
The RoleJoining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...
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...
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 translation of AI-designed oncology drugs from preclinical to clinical stages, focusing on biomarker and patient selection strategies.
As a Clinical Program Lead, you will provide strategic leadership and scientific rigor for global evidence generation programs, ensuring diagnostic solutions are backed by robust data to improve patient outcomes. You will drive the development of Integrated Evidence Generation Plans and oversee the delivery of complex global clinical trials, collaborating with cross-functional teams to align strategic decisions and manage program risks.
As a Clinical Program Lead, you will provide strategic leadership and scientific rigor for global evidence generation programs, ensuring diagnostic solutions are backed by robust data. You will drive the development of Integrated Evidence Generation Plans and oversee complex global clinical trials, collaborating with cross-functional teams to align on strategic decisions and manage program risks.
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...
Your work will change lives. Including your own.The Impact You’ll MakeWe are growing our chemistry team at Recursion and are seeking a Research Synthetic Chemist to join our Automated Chemistry group. We are looking for an individual that thrives in...
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 External Quality Assessment schemes, interpreting complex genomic data, and collaborating with senior scientific leaders and external partners to maintain high standards in diagnostic genomics.
The Scientific Programme Administrator will support the delivery of international genomics quality assurance schemes, ensuring diagnostic laboratories produce accurate genetic test results. Responsibilities include sample preparation, data handling, quality management, and logistics, with a focus on maintaining high standards and contributing to meaningful, impactful work.
