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Lead preclinical research in oncology cell biology to develop therapeutic strategies and advance drug programs. Collaborate with scientific teams to design experiments, interpret datasets, and support clinical development while contributing to regulatory submissions and the advancement of cancer research.
As a Senior Scientist in the Structural Biology and Protein Sciences Group, the candidate will perform gene-to-structure experiments, support antibody-drug conjugate projects, and collaborate across multi-disciplinary teams. Responsibilities include design, protein engineering, expression, purification, biophysical characterization, and structure determination.
The Associate Director of Biostatistics is responsible for designing, analyzing, and interpreting clinical trials and observational studies while ensuring compliance with regulatory requirements. This role involves providing statistical expertise for clinical development, regulatory submissions, and scientific reports, as well as fostering collaborations across clinical teams and leading statistical activities in study planning and execution.
The Senior Scientist will apply functional genomics and molecular biology expertise to accelerate drug discovery efforts. Key responsibilities include executing CRISPR screens, developing cellular models, and collaborating with interdisciplinary teams to investigate therapeutic mechanisms.
As a Principal Scientist, you'll leverage advanced solid-state analytical techniques to develop and evaluate pharmaceutical materials, ensuring drug quality and performance from discovery to commercial launch. You'll lead multidisciplinary teams, mentor junior scientists, and optimize drug formulations, fostering innovation in drug development.
As a Senior Scientist in Computational Materials Science, you will utilize advanced computational chemistry and crystallographic tools to predict molecular properties, guide drug design, and collaborate with multi-disciplinary teams to optimize new chemical entities for clinical trials and commercialization.
As an Associate Scientist, you will design and develop solid forms of active pharmaceutical ingredients and drug formulations, analyze powder samples, and apply various characterization techniques. You’ll utilize scientific knowledge to ensure chemical stability and manufacturability while collaborating with teams to convey experimental designs and results.
As a Principal Scientist, you will develop analytical strategies for pharmaceutical products, oversee method validation and stability studies, and lead project activities while collaborating with multidisciplinary teams. You will also author regulatory submissions and mentor peers in a commitment to high-quality standards.
As a Senior Principal Scientist, you will develop and implement cutting-edge analytical processes for biotherapeutics and vaccine products, ensuring they meet regulatory standards. You will contribute to multi-disciplinary teams, lead analytical strategy development, manage project timelines, and mentor junior scientists while ensuring quality and compliance throughout the drug development process.
The Clinical Data Scientist, Manager is responsible for overseeing clinical data operations, ensuring data accuracy and compliance, leading project teams, and collaborating with stakeholders. This role requires strong planning, data management skills, and the ability to guide operational teams in various projects to improve processes and facilitate data integrity.
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