As Lead Central Monitor, you will lead a team of Central Monitors, shaping monitoring strategies to ensure patient safety and data integrity in clinical trials. You will work across clinical, data, and risk-surveillance teams to translate complex risk signals into actionable insights and drive continuous improvement through analytics and technology.
As Lead Central Monitor, you will lead a team of Central Monitors, shape monitoring strategies, and ensure data integrity and patient safety in clinical trials. You will work across clinical, data, and risk-surveillance teams to translate complex risk signals into actionable insights and drive continuous improvement through analytics and technology.
This role involves providing end-to-end quality assurance and vigilance expertise for global and local pharmacovigilance activities. Responsibilities include driving regional quality oversight, ensuring compliance with regulations, and leading quality improvement initiatives.
The Associate Director, AI Product Manager supports the development, launch, and continuous improvement of AI-powered products. Key responsibilities include translating product vision, managing the product lifecycle, and ensuring alignment with user needs and business objectives through data-driven decision-making and ethical AI deployment.
This role involves leading early-phase clinical development (Phase 1 and 2) of novel gastroenterology therapies, with a focus on inflammatory bowel disease (IBD). The Translational Medicine Expert will design clinical development plans, serve as medical lead for trials, and collaborate closely with research, biomarker, and late-phase development teams. The position requires strong scientific leadership, engagement with key opinion leaders, and active involvement in regulatory interactions.
This role involves leading the identification, implementation, and scaling of innovative patient recruitment solutions for clinical trials. The director will work with global teams and technology partners to transform ideas into scalable capabilities, focusing on digital marketing and AI-driven approaches to improve patient engagement and trial participation.
This role involves leading the translational strategy for neurodegenerative programs, from preclinical research to early clinical development. Responsibilities include biomarker strategy, clinical trial design, and cross-functional leadership, with a focus on integrating patient-centered approaches and advancing scientific collaborations.
This role involves planning and executing high-quality medical and scientific engagement activities such as advisory boards, congress symposia, standalone meetings, and medical education programs across key therapeutic areas including Oncology, Cardiovascular Disease, and Neuroscience. The position ensures operational excellence by translating scientific strategies into actionable plans, managing cross-functional collaboration, and maintaining compliance with standardized processes. It plays a central role in improving workflows, vendor coordination, and continuous improvement within international medical affairs.
Lead statistical work across clinical trials, developing protocols, analysis plans, and reporting while driving innovative trial designs and methodologies. Collaborate with cross-functional teams including clinical, regulatory, and programming to support data-driven decision-making in drug development. Engage with external stakeholders such as health authorities and scientific communities to advance quantitative sciences in a pharmaceutical context.
This role involves managing clinical trial sites across Phase I–IV studies, ensuring protocol compliance, data integrity, and patient safety. The Clinical Research Associate conducts site visits, delivers training, monitors performance, and drives risk mitigation in collaboration with cross-functional teams. It is a field-based, site-facing position requiring strong regulatory knowledge and relationship-building skills.
This role involves leading early clinical pharmacology studies from protocol development to finalisation, ensuring high-quality data and informed program decisions. The Senior Clinical Pharmacology Trial Leader will work closely with internal teams, investigators, and CROs, overseeing study execution and risk management.
This role involves leading the identification, implementation, and scaling of innovative patient recruitment solutions for clinical trials. The director will work with global teams and technology partners to improve clinical trial participation, focusing on digital marketing and AI-driven approaches.
The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.
The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.
As Lead Central Monitor, you will lead a team of Central Monitors, shaping monitoring strategies to ensure patient safety and data integrity in clinical trials. You will work across clinical, data, and risk-surveillance teams to translate complex risk signals into actionable insights and drive continuous improvement through analytics and technology.
