Future Tech Jobs
Future Tech Jobs
The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust data analysis and regulatory compliance. They collaborate with cross-functional teams, manage external partners, and represent Biostatistics in regulatory interactions.
The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and ensure high-quality statistical insights.
This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic decisions, optimize investment, and collaborate across functions to deliver impactful patient outcomes.
This role involves owning and driving the global Oncology R&D strategy, setting priorities for the senior executive team, and transforming the approach to deliver impact for patients. The Executive Director will lead the creation of comprehensive therapeutic area strategies, provide strategic recommendations to senior leadership, and collaborate across functions to drive innovation and impact.
Leads Chemistry, Manufacturing and Controls (CMC) strategy and execution for small molecule, biopharm, or cell and gene therapy medicines from late-stage development through commercialisation. Oversees process development, regulatory filings, supply chain, and lifecycle management across global teams and external partners, ensuring readiness for approval and launch. Role involves high-level governance engagement, risk management, and transition to commercial supply.
The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global goals and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, anticipating risks, and driving timely submissions and approvals.
The Senior Scientific Writer II role involves developing high-quality medical and scientific communications for Novartis, including slide decks, congress materials, and advisory board content. The position requires strong collaboration with cross-functional teams to ensure content accuracy, consistency, and compliance with internal and external standards.
This senior role involves leading the scientific and operational aspects of complex, global early phase clinical trials. Responsibilities include designing and delivering high-quality studies, leading cross-functional teams, and ensuring robust data for key portfolio decisions. The role requires strong scientific and leadership skills, with a focus on continuous improvement and team collaboration.
This role involves leading high-parameter spectral flow cytometry activities in a GCLP-compliant clinical laboratory, generating immunophenotyping and functional immune profiling data from PBMC and whole blood samples to support mRNA-based clinical development. The scientist will independently execute and analyze complex assays, contribute to assay development and validation, and ensure regulatory compliance while leveraging advanced platforms like the Cytek Aurora. Opportunities exist to engage with digital tools and generative AI for data interpretation and workflow optimization within a collaborative, innovation-driven environment.
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...
This role involves managing the non-clinical aspects of IND submissions, including CMC, DMPK, pharmacology, and tox reporting. You will create and maintain detailed project plans, manage data and document workflows, and coordinate cross-functional teams to ensure regulatory compliance and successful submission.
Lead a team of computational biologists to integrate multi-omics data for oncology target discovery and validation, while actively contributing to analyses and mentoring team members. Drive biomarker strategy and patient stratification to advance precision oncology programs. Collaborate closely with biologists, chemists, and clinical teams to deliver data-driven insights that accelerate drug development.
The Disease Level Partner (DLP) is responsible for implementing Roche's strategy and objectives within therapy areas, focusing on patient outcomes. Key responsibilities include deep customer engagement, gathering actionable insights, and driving positive customer experiences. The role involves leveraging resources to secure access for key customers and contributing to the development of local and national brand advocates.
This role involves evaluating current clinical assay performance monitoring methods and designing a digital solution to improve standardization and visibility across laboratory teams. The intern will work with real datasets and collaborate with scientists to prototype tools for tracking assay performance, potentially incorporating AI-driven insights. The position offers hands-on experience in a regulated clinical environment and cross-functional stakeholder engagement.
As a Synthetic Chemistry Lead, you will apply your expertise to drive medicinal chemistry and CMC projects, collaborating with multidisciplinary teams and external partners. You will play a key role in advancing drug discovery programs and representing the company to collaborators, while fostering a culture of inclusion and continuous development.
