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IQVIA

Project Manager, Remote Research Clinicians

Posted 2 Days Ago
Be an Early Applicant
In-Office or Remote
Hiring Remotely in Reading, Berkshire, England
Senior level
In-Office or Remote
Hiring Remotely in Reading, Berkshire, England
Senior level
Manage global clinical research projects, ensuring quality and adherence to timelines while collaborating with sponsors and sites.
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Bring clinical research directly to patients - and make a real-world impact

At IQVIA, we are driven by a single purpose: to help improve patients’ lives by accelerating the development and delivery of innovative healthcare solutions. Our Remote Research Clinicians (RRC) model is transforming how clinical trials are delivered - bringing high‑quality clinical services directly to patients, wherever they are.

We are looking for an experienced Project Manager, Remote Research Clinicians to lead complex, protocol‑driven projects and ensure seamless delivery across sponsors, sites, clinicians, and internal teams.

About the role

In this role, you will take full ownership of a portfolio of global RRC projects, acting as the primary point of contact for key stakeholders while operating with a high degree of independence. You will provide end‑to‑end project oversight - from planning and financial management through execution, quality, and delivery -ensuring an exceptional experience for sponsors, sites, clinicians, and patients alike.

You will work closely with cross‑functional internal teams and external partners, delegating visit coordination activities to Regional Specialists and guiding teams toward successful milestone achievement.

What you’ll be doing

  • Lead and deliver a portfolio of global Remote Research Clinicians projects with full accountability for quality, timelines, and outcomes

  • Serve as the primary interface with Sponsors, Sites, and clinicians, building trusted and effective working relationships

  • Manage project finances, including budget development, forecasting (EAC), invoicing, scope alignment, and change control

  • Develop and maintain key project documentation such as project plans, trackers, presentations, and stakeholder communications

  • Identify and proactively manage risks, issues, and quality concerns, implementing corrective and preventive actions as needed

  • Build, lead, and mentor cross‑functional project teams, fostering collaboration and supporting professional development

  • Track, analyze, and report project metrics to support informed decision‑making

  • Identify opportunities to optimize delivery, accelerate activities, and implement best practices across projects

  • Act as a change advocate, supporting corporate initiatives and continuous improvement efforts

What you’ll bring

  • Bachelor’s degree in Life Sciences or a related field

  • At least 5 years of relevant experience in clinical research, including 2+ years in a Project Manager role

  • Hands‑on experience working directly with clinical research sites

  • Solid understanding of clinical trial conduct, including ICH‑GCP and applicable regulatory requirements

  • Experience with remote visits and clinicians (e.g., RN, RD, phlebotomist) is highly desirable

  • Strong stakeholder management, communication, and organizational skills

  • Fluent written and spoken English

  • Based in the UK

Why IQVIA

You’ll join a global organization at the forefront of clinical innovation, where your work directly contributes to improving patient access to research and care. At IQVIA, we value collaboration, ownership, and curiosity - and we’re committed to supporting your growth every step of the way.

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. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Top Skills

Budget Management
Clinical Trial Management
Ich-Gcp
Project Management
Regulatory Requirements

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