Lead clinical pharmacology, modeling, and simulation efforts for infectious disease assets, driving dose selection and development strategy through population PK/PD and exposure-response modeling. Serve as a scientific leader within cross-functional teams while remaining hands-on with quantitative analyses. Contribute to regulatory submissions and advance model-informed drug development across the R&D lifecycle.
Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying quantitative methods to inform dose selection, trial design, and regulatory strategy. Work across development phases from early planning to lifecycle management, using population PK/PD and exposure-response modelling. Operate as a scientific leader within a cross-functional environment while remaining hands-on with data analysis and model development.
Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.
As a Security Engineering Manager, you will lead and scale a high-performing team responsible for securing Isomorphic Labs' AI-driven drug discovery platform. You'll define the technical security roadmap across cloud infrastructure, IAM, secure SDLC, and security monitoring, while enabling rapid innovation for ML researchers and drug discovery teams. The role involves pioneering AI-first security architectures, leading transformational projects, and acting as a key liaison within the Alphabet/Google ecosystem.
This role involves managing regulatory maintenance activities for a high-complexity pharmaceutical product portfolio, ensuring compliance and timely submissions to global health authorities. The individual will lead strategic regulatory input across cross-functional teams, respond to complex queries, and support continuous process improvements. It is a hybrid or remote position with a focus on lifecycle management of innovative medicines.
Leads the development and maintenance of global labelling strategies and core documents for pharmaceutical products, ensuring scientific accuracy and regulatory compliance. Facilitates cross-functional alignment, supports health authority interactions, and mentors team members. Focuses on consistent, competitive product information across global markets.
This role involves pioneering research in synthetic biology, focusing on genome synthesis and genetic isolation to enable safe, scalable biotechnological applications. The postdoctoral fellow will develop novel methods for genome recoding, engineer synthetic genetic codes, and contribute to foundational work in making biology programmable. Work integrates experimental and computational approaches within a multidisciplinary, mission-driven research environment.
Design and develop generative protein models that capture enzyme dynamics and function, with a focus on catalysis through motion. Analyze complex datasets and collaborate with interdisciplinary teams to evolve designs in vivo. Contribute to high-impact research publication and translation within a cutting-edge synthetic biology environment.
Leads CSL's engagement in the Northern Europe and UK biotech innovation ecosystems, building strategic relationships with academia, biotech firms, and investors to identify and drive partnership opportunities. Acts as a senior deal team member, sources external innovation aligned with therapeutic area priorities, and represents CSL at industry events and boards. Requires deep regional network expertise and collaboration with global R&D and business development teams to strengthen the company’s innovation pipeline.
This role leads global clinical strategy for Roche’s toxicology and drug testing portfolio, driving clinical development programs from concept to registration. The Clinical Development Leader will design evidence generation plans, engage with regulatory authorities, integrate real-world data, and collaborate with KOLs to advance diagnostic solutions. They will also mentor team members and shape scientific communication to support product adoption and innovation in clinical toxicology.
Process environmental samples through DNA extraction, normalization, and library preparation pipelines using automated systems and manual techniques. Perform QC checks, maintain LIMS records, and support R&D protocol testing in a high-throughput, CL2-compliant lab environment. Contribute to maintaining a safe, organized workspace and enable scalable data generation for AI-driven biological discovery.
Develops and optimizes metagenomic extraction and sequencing workflows for diverse sample types, focusing on low-biomass and inhibitor-rich matrices. Works end-to-end from DNA/RNA extraction to library prep, with emphasis on high molecular weight recovery and virology applications. Collaborates globally to enhance data quality and scalability for AI-driven biological discovery.
Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.
This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.
