Clinical Study Lead - Global Trials & CRO Oversight

Ipsen; Greater London; On-site; GBP 107,000 - 149,000; Full time

Job summary

Ipsen Biopharmaceuticals Inc. is seeking a Clinical Project Manager to lead cross-functional clinical study teams and manage global trial activities from start-up to CSR in a regulated environment.

You will oversee study budgets, timelines, CRO relationships, and regulatory compliance, ensuring quality and timely delivery. Applicants should have a Bachelor’s in life sciences and at least 3 years in clinical research, with 2+ years in management.

Qualifications

• Bachelor’s degree in life science or medical graduate preferred.
• Minimum of 3 years working in clinical research with management of clinical activities for international registrational studies, for at least 2 years.
• Experience in managing and developing relationships with CROs/SPs.
• Fluent English; excellent leadership and team management in a regulated environment.
• Knowledge of GCP or other clinical study regulations (ICH E6, EU Directive).
• Strong organizational and budgeting abilities; ability to work in a matrix environment.

Responsibilities

• Lead cross-functional clinical study teams focused on conduct of assigned projects.
• Interact with CDPD to define strategic operational direction.
• Review status reports and highlight issues to facilitate decision making.
• Manage and lead all operational aspects for implementation and conduct of global clinical trial activities from start-up to CSR.

Skills

Fluent English

Leadership

Project management

Budgeting

Regulatory knowledge

Cross-functional teamwork

Education

Bachelor’s degree in life science

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Adobe Reader

Job description

Ipsen Biopharmaceuticals Inc. is seeking a Clinical Project Manager to lead cross-functional clinical study teams and manage global trial activities from start-up to CSR in a regulated environment.

You will oversee study budgets, timelines, CRO relationships, and regulatory compliance, ensuring quality and timely delivery. Applicants should have a Bachelor’s in life sciences and at least 3 years in clinical research, with 2+ years in management.