The Senior Principal Statistical Programmer will lead the design, development, and validation of SAS programs for clinical trial deliverables while ensuring compliance with CDISC and regulatory standards. This role also involves collaborating with cross-functional teams and bridging clinical programming efforts with AI infrastructure.
The software engineer will build and maintain Python applications and cloud workflows to support computational chemists and machine learning researchers. They will also be responsible for orchestrating, monitoring, and troubleshooting scientific workloads on AWS and other cloud platforms.
The Lead Clinical Data Manager directs data management activities across the full study lifecycle, from start-up through database lock. They provide project-level leadership, oversee CRO and EDC vendor performance, and ensure compliance with regulatory standards.
The Associate Director will oversee outsourced pharmacovigilance activities and manage safety deliverables across all phases of clinical development. They will collaborate with cross-functional teams to ensure regulatory compliance, inspection readiness, and effective vendor performance monitoring.
The Associate Medical Director/Medical Director will serve as the medical monitor for phase 1 clinical trials, ensuring patient safety and regulatory compliance. They will also collaborate with cross-functional teams to drive clinical program strategy and support IND submission preparations.
Design and build agentic systems that automate the acquisition, cleaning, and quality control of large-scale biomedical datasets. Collaborate with ML scientists to maintain production data pipelines and ensure data provenance and reproducibility.
The Principal Medical Writer will independently author and oversee the development of submission-ready clinical documents such as protocols, IBs, and CSRs. They will also lead cross-departmental collaboration and help refine medical writing processes and AI-enabled workflows.
The Senior Clinical Trial Manager provides end-to-end operational leadership for early-phase oncology studies from start-up through close-out. This role manages cross-functional teams, vendor performance, and study budgets while ensuring compliance with global regulatory requirements.
The Research Scientist will apply ligand and structure-based computational techniques to support drug discovery efforts across hit identification and lead optimization. They will collaborate with cross-functional teams to integrate machine learning models and structural hypotheses into actionable molecular designs.
Serve as the primary relationship lead for AI-enabled drug discovery collaborations and strategic external partnerships. Coordinate cross-functional teams to ensure alignment on scientific, operational, and strategic objectives while managing governance and deliverables.
Serve as the primary relationship lead for external drug discovery collaborations, managing governance and cross-functional execution. Coordinate between scientific teams and partners to ensure programs advance from early discovery through preclinical development.
Serve as the primary finance business partner for Discovery R&D groups to lead financial planning, forecasting, and budgeting for internal and external programs. Provide detailed analytics and actionable insights to senior leadership to support strategic decision-making and long-range planning.
