Global Study Manager

i-Pharm Consulting
London
8 months ago
Applications closed

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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 aStudy Managerto 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 todayand be part of a team that’s changing the future of healthcare!

Seniority level

  • Seniority levelMid-Senior level

Employment type

  • Employment typeContract

Job function

  • Job functionScience and Health Care Provider
  • IndustriesPharmaceutical Manufacturing, Biotechnology Research, and Public Health

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