Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe)

IQVIA; Reading; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization is seeking a Global Trial Manager to oversee late-phase global clinical trials. The role involves managing trial budgets, developing study tools, and collaborating with internal teams to ensure successful trial delivery. Candidates should have an advanced degree in life sciences and experience in project management. This position is home-based in Europe and requires a passion for late-phase studies.

Qualifications

• 2-5 years managing late-phase global clinical trials.
• Experience with non-interventional, post-marketing, and safety studies.
• Understanding of Good Clinical Practice and drug development process.

Responsibilities

• Develop protocol sections and study tools.
• Oversee trial budgets and support drug supply management.
• Organize trial committees and coordinate with internal functions.

Skills

Excellent communication

Project management

Vendor management

Collaboration

Regulatory safety documentation

Education

Advanced degree in life sciences or healthcare

Job description

Job Title: Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe), Reading

Client: IQVIA

Location: Reading, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: e63721864143

Job Views: 41

Posted: 12.08.2025

Expiry Date: 26.09.2025

Job Description:

Job Purpose: As Senior Global Trial Manager, you will contribute to all aspects of assigned clinical trials to ensure successful delivery within schedule, budget, and quality standards. You will lead specific aspects of global trials and be a core member of the Clinical Trial Team (CTT).

Key Responsibilities:

• Study essential documents: Develop protocol sections, study tools, guidelines, training materials, contribute to CRF development, data review, and regulatory documents.
• Project Management: Report trial results, support drug supply management, oversee trial close-out activities, manage trial budgets, and participate in data review plans.
• Vendor Management: Develop outsourcing specifications, manage CRO interfaces, ensure quality standards, and manage vendor contracts.
• Collaboration: Organize trial committees, act as site contact, coordinate with internal functions, and report on trial progress.

Ideal Background:

• Advanced degree in life sciences or healthcare preferred.
• 2-5 years managing late-phase global clinical trials.
• Experience with non-interventional, post-marketing, and safety studies.
• Knowledge of regulatory safety documentation and clinical trial design.
• Excellent communication, organization, and networking skills.
• Understanding of Good Clinical Practice and drug development process.
• Passion for late-phase studies.

IQVIA is a leading provider of clinical research and healthcare insights. We value diversity, inclusion, and belonging, fostering a culture where talented employees can thrive and innovate.