Regulatory Affairs Manager role involves developing EU regulatory strategies, overseeing clinical study submissions, and ensuring compliance with EU legislation.

Manage HCP engagement and contracting operations, providing training and compliance guidance while optimizing processes in the pharmaceutical sector.

Manage International Payroll operations, ensuring compliance with local regulations, oversee payroll processing, reporting, and implement payroll systems for multiple countries.

The Director, Program Operations Leader oversees clinical operations for trials, ensuring quality, timelines, and budgets are met. Responsibilities include management of staff, budget oversight, stakeholder communication, and operational insights on clinical program development.

The Senior Clinical Study Lead manages global execution of complex clinical trials, ensuring compliance, budget management, and process improvement while leading teams and overseeing vendor engagement.

The Senior Clinical Study Lead is responsible for the global execution of complex clinical trials, ensuring compliance, managing study timelines and budgets, overseeing vendor engagements, and leading the clinical study teams.

The Senior Manager, Regulatory Affairs will develop regulatory strategies, oversee submission of Clinical Trial Applications, and ensure compliance with EU regulations, focusing on metabolism and ophthalmology.

The Senior Manager will optimize the Site Start-Up team by enhancing tools and processes, facilitating improvements, reporting, and innovation in clinical trials.