Global Study Manager

i-Pharm Consulting; London; On-site; GBP 50,000 - 80,000; Full time

Job summary

Join a leading company as a Global Study Manager in London, driving impactful clinical studies for rare genetic diseases. You'll lead cross-functional teams, manage study lifecycles, and ensure high-quality results. This role is ideal for experienced professionals passionate about clinical research and healthcare innovation.

Qualifications

• 7+ years in life sciences, including 4 years in clinical research.
• Experience managing external vendors highly valued.

Responsibilities

• Oversee execution of clinical studies ensuring quality and compliance.
• Manage entire study lifecycle from start-up through close-out.
• Monitor study metrics, timelines, and budgets.

Skills

Leadership

Problem-solving

Communication

Job description

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!

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Science and Health Care Provider

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Public Health

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