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Global Study Manager

i-Pharm Consulting
London
1 week ago
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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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