Global Clinical Trials Regulatory Officer

Thermo Fisher Scientific is seeking a Senior Staff Regulatory Affairs Specialist to interpret and disseminate global regulations while collaborating with cross-functional teams to bring innovative products to market. You will contribute to regulatory strategies, maintain lifecycle compliance, and support improvements to regulatory tools, enabling patient...

Thermo Fisher Scientific is seeking a Senior Staff Regulatory Affairs Specialist to interpret and disseminate global regulations while collaborating with cross-functional teams to bring innovative products to market. You will contribute to regulatory strategies, maintain lifecycle compliance, and support improvements to regulatory tools, enabling patient...

IQVIA is seeking a Global Feasibility Specialist to support clinical systems and tools used by Development Operations. You will work with study teams to identify sites, set up feasibility processes, and provide data-driven inputs to optimize site selection for clinical studies. In this role, you will analyze data, coordinate with stakeholders, and stay...

IQVIA is seeking a senior Medical Writer to deliver high-quality clinical documents for eye health and inflammatory indications. You will integrate with sponsor teams, manage timelines, and ensure adherence to regulatory requirements across ICH, FDA, and EMA guidelines. The role emphasizes senior-level writing leadership, collaboration across disciplines,...

Worldwide Clinical Trials is seeking a Clinical Data Manager to lead data management activities across global trials, from start-up to database lock. You will coordinate resources, develop essential trial documents, and ensure data integrity throughout the lifecycle.The role requires a minimum of 3 years in clinical data management, strong English, and the...

Johnson & Johnson is currently seeking a Manager, Cross Therapeutic Area Clinical Risk Management to join our R&D Quality CRM team located at a J&J office in Spring House, PA; Titusville, NJ; Raritan, NJ; Beerse, Belgium; and Basel, Switzerland. About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose...

IQVIA's Global Site Activation team in Spain seeks a Senior Site Activation Specialist to lead complex projects and serve as a single point of contact for investigative sites and project teams. You will ensure SOPs and timelines are followed, perform feasibility, site ID, start-up, and activation activities, and review documents for completeness and...

A leading clinical research organization is looking for a Senior Clinical Research Associate in Madrid. The successful candidate will oversee clinical trial activities ensuring compliance with protocols and regulatory standards. Key responsibilities include monitoring trial sites, conducting visits for performance assessment, and ensuring data integrity....

Global Study Leadership is seeking a Clinical Lead to oversee the clinical delivery of assigned studies across regions, ensuring recruitment, site performance, quality and regulatory compliance. You will work with Project Leaders and cross-functional teams to drive milestones, resolve issues and maintain operational excellence, using AI-enabled insights and...