Future Tech Jobs
Future Tech Jobs
CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.1 Lead full scope...
The Medical Director, Oncology Clinical Development will lead clinical research activities for GSK’s oncology portfolio, collaborating with various stakeholders to develop and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key external experts.
The Medical Director, Oncology Clinical Development, will lead clinical research activities to advance GSK’s oncology portfolio. Key responsibilities include developing and executing phase 1-3 clinical trials, collaborating with cross-functional teams, and engaging with key external experts to ensure the successful development and regulatory approval of innovative oncology treatments.
This role involves project managing and tracking the ClinTech roadmap, working closely with Clinical Development Operations and Decision Science to translate priorities into actionable plans. You will also support the communication of ClinTech’s progress to senior leadership and external audiences, contributing to vendor assessments and build-vs-buy evaluations. The role is at the heart of a high-visibility team building a platform to accelerate drug development.
Your work will change lives. Including your own.The Impact You'll MakeRecursion is at the forefront of reimagining drug discovery by integrating technological innovations across biology, chemistry, automation, data science, and engineering to radically improve lives by industrializing drug discovery. We...
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 the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic development of GSK's oncology portfolio.
The Medical Director, Oncology Clinical Development, will lead the development and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic direction of GSK's oncology portfolio.
The Medical Director, Oncology Clinical Development, will lead the development and execution of clinical trials for hematological malignancies, collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance. This role involves medical monitoring, data review, and strategic partnerships with thought leaders.
The Medical Director, Oncology Clinical Development, will lead the development and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic direction of GSK’s oncology portfolio.
This role involves leading the development and execution of precision diagnostics strategies for oncology programs, working cross-functionally with research, clinical, regulatory, and commercial teams. Responsibilities include defining diagnostic requirements, overseeing project plans, and engaging external partners to accelerate assay development and regulatory submissions.
This role involves leading a team responsible for the development, deployment, support, and maintenance of IT systems used in the R&D clinical supply chain. The Director will ensure systems align with business strategies, regulatory requirements, and drive innovation and efficiency.
This role involves leading the RTSM function in the US, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, risk assessments, process improvements, and fostering collaboration across internal and external partners.
This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing global medical teams, managing external partnerships, and ensuring scientific quality and compliance.
