Overview As Clinical Development Lead for CRM, you will own the strategic and operational direction of the clinical development plan for this asset in Germany. You will guide a team of clinical leaders to execute a data-driven program
Overview As Senior Clinical Program Lead, you will drive phase II–III development for obesity and liver diseases within a newly formed Global Clinical Development group. You will steer cross-functional teams to deliver high-quality trial execution and shape regulatory
Overview In this role you coordinate investigator grants and contracting activities to support proposal development and trial initiation. You will maintain contracting systems, produce specialist contract language, and align with sponsor requirements and RSU plans. You’ll collaborate
Overview In this role, you will lead clinical trial operations for sponsor-specific partnerships in Germany, overseeing site and central monitoring with a focus on patient safety and data integrity. You will collaborate with cross-functional teams to
Overview In this role you drive the design and execution of early-stage oncology clinical development plans, leading cross-functional teams to translate strategy into patient-ready programs. You will shape trials, contribute to regulatory and Medical Affairs strategies, and
Overview Senior Statistician at Viatris leads statistical design and strategy for clinical studies, ensuring high scientific and regulatory quality. You partner with clinical science, operations, regulatory teams, and CROs across multiple therapeutic areas. You drive methodological
Overview In this role, you drive early-phase obesity and liver programs from strategy through execution, leading cross-functional teams to advance therapies. You’ll influence regulatory strategy and contribute to Medical Affairs plans, shaping evidence generation and decision-making
Overview As a Project Manager in Medical Writing, you lead and develop a capable team to deliver compliant, high-quality medical writing outputs within sponsor partnerships. You align with clinical development objectives and collaborate across functions to shape
Overview In this role you lead trial monitoring staff (CRAs) within the country to ensure high-quality clinical trial execution. You work closely with the Regional Clinical Operations Manager to meet study timelines and quality standards, while