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The Clinical Project Manager II will oversee clinical trials, manage study timelines, ensure compliance with regulations, and coordinate cross-functional teams.

The role involves overseeing clinical trials, creating project plans, managing budgets, ensuring compliance with regulations, and developing recruitment strategies.

Manage interdisciplinary clinical research projects, ensuring compliance with regulations, overseeing project delivery and liaising with clients while driving financial performance and managing project teams.

The Project Manager II coordinates clinical study timelines, collaborates with teams, ensures compliance with regulations, oversees operational aspects of trials, and develops recruitment strategies for successful enrollment.

Manage and coordinate clinical research studies, ensuring compliance with regulations, maintaining study documentation, and facilitating communication among stakeholders.

The Single Sponsor Payment Specialist will assist in site management activities, maintain clinical tracking information, and coordinate supplies for assigned studies, ensuring compliance with protocols and guidelines.

Manage clinical trial sites, ensure compliance with regulations, assess site performance, conduct monitoring visits, and optimize site activities throughout the trial lifecycle.

Assist in governance meetings, draft minutes, proofread labeling documents, ensure compliance in labeling processes, and manage templates.

This role involves performing clinical data reviews for quality assurance, managing queries in EDC systems, collaborating with stakeholders, and ensuring GCP compliance.

The Principal Biostatistician leads biomarker-related statistical activities in clinical studies, develops evaluation plans, and performs complex data analysis, focusing on genomics and biomarkers.