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The CRA II conducts site qualification, monitoring, and management activities ensuring compliance with regulatory standards and protocols, while communicating with site staff and managing study progress.

The Director of Epidemiology Pipeline collaborates on virology clinical trials, providing scientific expertise, leading project proposals, and overseeing study management and regulatory compliance.

The role involves managing clinical research projects, ensuring compliance with regulations, coordinating teams, overseeing budgets, and developing client relationships, while providing leadership and training to staff.

The Internal Account Director will lead patient recruitment and retention strategies for clinical trials, ensuring successful enrollment and collaboration with various stakeholders.

The role involves applying quality management expertise in a clinical setting, working collaboratively in a team to ensure effective drug development solutions.

The Principal Biostatistician leads biomarker analysis for clinical studies, develops evaluation plans, conducts data analyses, mentors staff, and ensures accurate statistical deliverables while collaborating across teams.

The role involves managing project files, ensuring compliance with guidelines, providing administrative support, maintaining communication among team members, and assisting in quality assurance activities.

The role involves site management in clinical trials, including site qualification, monitoring, compliance verification, data accuracy, and communication with site staff to ensure regulatory standards are met.

The role involves programming and data review for real-world data analysis, supporting epidemiologists, and managing complex data sets using statistical programming languages and tools.

Responsible for site qualification, management activities, and ensuring compliance with regulations and protocols for clinical studies.