Global Study Manager

JR United Kingdom; Slough; On-site; GBP 55,000 - 85,000; Full time

Job summary

Join a leading global company as a Global Study Manager in London, where you will oversee impactful clinical studies that change patients' lives. This role requires strong leadership and problem-solving skills to navigate the complexities of clinical research in a fast-paced environment.

Qualifications

• 7+ years in life sciences, with at least 4 years in clinical research.
• Experience managing external vendors is highly valued.
• Strong ability to manage complex studies.

Responsibilities

• Oversee execution of critical clinical studies.
• Manage study lifecycle from start-up to close-out.
• Monitor study metrics, timelines, and budgets.

Skills

Leadership

Problem-solving

Communication

Job description

Social network you want to login/join with:

Exciting Opportunity: Study Manager, Global Study Operations – Make an Impact on Patients' Lives!

Job Title: Global Study Manager

Location: London

Employment type: Full-Time

We are looking for a Study Manager to join the team and help drive impactful clinical studies that change lives. You will be working with a global leader in developing innovative therapies for rare genetic diseases, dedicated to transforming the lives of patients with serious and life-threatening conditions.

If you're passionate about clinical research and want to be a part of a dynamic team that’s changing the future of healthcare, we want to hear from you!

What You’ll Do:

As a Study Manager in the Global Study Operations team, you’ll oversee the execution of critical clinical studies that are integral to delivering life-changing treatments. You’ll be the key leader driving the study’s success, ensuring it stays on track, within budget, and delivers high-quality results.

• Lead with Impact: You will be the primary point of contact for your study, guiding cross-functional teams, managing external vendors, and ensuring timely and successful study deliverables.
• Drive Study Success: Manage the entire study lifecycle—from start-up through close-out—while maintaining high standards for quality and compliance.
• Collaborate and Influence: Facilitate Study Execution Team (SET) meetings, work closely with cross-functional stakeholders, and address risks and opportunities proactively.
• Deliver Results: Monitor study metrics, timelines, and budgets while providing regular progress updates to stakeholders, ensuring the study progresses smoothly.

Who You Are:

You are an experienced and proactive clinical research professional who thrives in a fast-paced, dynamic environment. You have a strong ability to manage complex studies and work with diverse teams to deliver exceptional results.

• Experience: 7+ years in life sciences, including at least 4 years of clinical research experience in biotech, pharma, or CRO settings. Experience managing external vendors is highly valued.
• Skills: Strong leadership, problem-solving, and communication skills. You’re skilled at navigating complex situations and making sound decisions.
• Knowledge: In-depth understanding of clinical trial processes, regulatory requirements, and drug development.

Apply today and be part of a team that’s changing the future of healthcare!