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

IQVIA; Reading; On-site; GBP 65,000 - 85,000; Full time

Job summary

A global clinical research provider is seeking an experienced Senior Global Trial Manager in Reading, UK. This role involves managing late-phase clinical trials, overseeing data and project leadership, and collaborating with multiple stakeholders. Candidates should have an advanced degree and 2–5 years of relevant project experience. This position emphasizes strong protocol development and trial coordination skills within a diverse and inclusive environment.

Qualifications

• 2–5 years' global experience managing phase IV, PASS, PAES, or NIS trials.
• Strong track record in protocol development, study startup, and regulatory writing.
• Deep understanding of GCP and clinical trial design.

Responsibilities

• Lead cross-functional collaboration with data management and drug supply.
• Oversee data review and TMF audit readiness.
• Support study closeout and issue resolution.

Skills

Protocol development

Study startup

Regulatory writing

Collaboration skills

Communication skills

Education

Advanced degree in life sciences

Job description

Senior Global Trial Manager – Single Sponsor (Novartis)

Are you experienced in managing late phase clinical trials at a global level?

We are looking for a Senior Global Trial Manager to join our Single Sponsor Department, dedicated exclusively to Novartis.

Join our global team and take ownership of delivering late-phase clinical trials that meet timelines, budgets, and quality standards. As a core Clinical Trial Team (CTT) member, you'll lead critical aspects of global studies and collaborate across functions to drive success.

As part of your role, you’ll have the opportunity to specialise in one of the following areas:

• Scientific Review Committee (SRC)
• Non-Interventional Studies (NIS)
• Managed Access Programs (MAP)
• Investigator-Initiated Trials (IITs)
• Research Collaborations (RCs)
• Program Level Documents (PLD)

Key Responsibilities

Clinical Documentation & Study Tools

• Draft sections of protocols, CRFs, training materials, and data review plans
• Contribute to the development of safety updates, IBs, and regulatory submissions

Project Leadership

• Oversee data review and TMF audit readiness
• Forecast/manage investigational product supply
• Support study closeout, issue resolution, and lifecycle budget tracking
• Contribute to Managed Access Program coordination and compliance

Vendor & Stakeholder Management

• Coordinate CRO/vendor selection and performance
• Facilitate advisory boards (DMCs/Steering Committees) and serve as the site liaison
• Lead cross-functional collaboration with data management, drug supply, and more

What You'll Bring

• Advanced degree in life sciences or healthcare
• 2–5 years' global experience managing phase IV, PASS, PAES, or NIS trials
• Strong track record in protocol development, study startup, and regulatory writing (e.g. PSURs, DSURs, NDA/BLA reports)
• Excellent communication, organizational, and collaboration skills
• Deep understanding of GCP and clinical trial design
• Passion for advancing real-world evidence and patient outcomes

This role is not eligible for UK VISA sponsorship.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere.