The Medical Writer III role involves writing and coordinating clinical and regulatory documents, leading cross-functional document planning meetings, and mentoring junior staff. The position is hybrid, with 3 days onsite weekly, and may be located in multiple European countries.
This role involves writing and coordinating clinical and regulatory documents, leading cross-functional document planning and review meetings, and mentoring junior staff. The position is hybrid, with 3 days onsite weekly, and supports key therapeutic areas within the Integrated Data Analytics & Reporting (IDAR) business.
Develops and oversees clinical data programming for complex trials, creating CDISC-compliant SDTM datasets and define.xml, implementing data mappings, edit checks, and custom safety/compliance reports. Focuses on data quality, regulatory standards, and integration of diverse clinical data sources to support trial oversight and submissions.
The Service Manager Capital and VELYS role involves leading a team to support service and repair activities, ensuring high customer satisfaction, and managing technical service activities such as installations, maintenance, and software upgrades. The role also includes developing and implementing process improvements and coaching team members.
The Clinical Trial Assistant supports the Local Trial Manager and Site Manager in managing clinical trial documents and logistics. Responsibilities include administrative tasks, ensuring compliance with regulations, and contributing to process improvements and training.
The Senior Process Engineer is responsible for optimizing manufacturing value streams, leading process development and validation, and driving continuous improvement initiatives. The role involves strategic technical leadership, mentoring junior engineers, and ensuring compliance with quality and regulatory standards.
Leads environmental, health, safety, and Process Safety Management (PSM) programs at a manufacturing site, ensuring regulatory compliance and driving a strong safety culture. Focuses on risk-based safety integration, incident investigation, and continuous improvement in regulated environments. Serves as a key advisor to leadership on safety strategy and regulatory interactions.
The Sr. Manager, Safety/PSM role involves leading and managing global safety and Process Safety Management (PSM) programs, ensuring compliance with regulations, and driving a strong safety culture. Key responsibilities include developing safety policies, conducting audits, and partnering with site leadership to mitigate risks.
The Sr. Manager, Safety/PSM leads and manages global safety and Process Safety Management (PSM) programs, ensuring compliance with regulations and driving a strong safety culture. Key responsibilities include leading safety audits, developing safety policies, and partnering with site leadership to mitigate risks.
Leads environmental, health, and safety (EHS) and Process Safety Management (PSM) programs at a manufacturing site, ensuring regulatory compliance and driving a strong safety culture. Responsibilities include managing PSM elements such as hazard analysis, management of change, and incident investigation, while partnering with operations and leadership to mitigate risks. Focuses on continuous improvement of safety systems and performance through data analysis, audits, and cross-functional collaboration.
The Sr. Manager, Safety/PSM leads and manages global environmental, health, safety, and Process Safety Management (PSM) programs. Key responsibilities include ensuring regulatory compliance, driving a strong safety culture, and integrating risk-based safety practices into manufacturing and operational activities.
This role involves leading a focused research program on AI safety in pharmaceutical R&D, specifically in provable controls, adversarial assurance, and safety-native architecture. You will design experiments, prototype solutions, and work with engineering teams to integrate validated methods into the GenAI platform.
This role involves leading a focused research program on AI safety in pharmaceutical R&D, specifically in provable controls, adversarial assurance, and safety-native architecture. You will design and execute experiments, prototype systems, and work with engineering teams to integrate validated methods into the GenAI platform.
This role involves leading a focused research program on AI safety in pharmaceutical R&D, specifically in provable controls, adversarial assurance, and safety-native architecture. You will design and execute experiments, prototype systems, and collaborate with engineering teams to integrate validated methods into the GenAI platform.
This role involves leading a focused research program on AI safety in pharmaceutical R&D, specifically in provable controls, adversarial assurance, and safety-native architecture. The researcher will design experiments, prototype systems, and work with engineering teams to integrate validated methods into the GenAI platform.
