Clinical Project Manager

TN United Kingdom; Chesterfield; Remote; GBP 40,000 - 70,000; Full time

Job summary

An innovative firm is seeking a Clinical Project Manager to lead local studies and coordinate clinical trials from start-up to close-out. This role offers the chance to work on groundbreaking medicines while collaborating with talented colleagues. With options for remote, hybrid, or office-based work, you'll manage study timelines, budgets, and site selection, ensuring compliance with ICH-GCP and local regulations. Join a team dedicated to advancing healthcare and enjoy genuine career development opportunities in a supportive environment.

Benefits

Career development opportunities

Access to extensive data pools

Innovative medicines projects

Qualifications

• 2-3 years of clinical trial project management experience.
• Knowledge of ICH/GCP guidelines and clinical trial processes.

Responsibilities

• Oversee local studies and manage operational aspects of clinical trials.
• Partner with teams to ensure study delivery and execution.

Skills

Clinical monitoring

Project management

Team leadership

Clinical trial processes

Budget management

Education

Bachelor’s degree in healthcare

Job description

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Clinical Project Manager

Sponsor Dedicated, Home Based, UK

Join us on our exciting journey!

Remote/Hybrid/Office based working options.

Our Sponsor Dedicated (cFSP) team is growing. Join us on our mission to advance healthcare!

Role Overview:

As a Clinical Project Manager, you will oversee local studies across therapeutic areas, managing operational aspects to meet contractual requirements. You will serve as the main contact to lead, manage, and coordinate clinical trials from start-up (COLA) to close-out, in accordance with ICH-GCP and local regulations.

Key Responsibilities:

1. Partner with global and local teams to develop country strategies, drive study progress, and ensure study delivery at the country level.
2. Plan, manage, and oversee clinical study execution following the global strategy through leadership of the Local Study Team (LST).
3. Support operational planning at the country level and be responsible for site selection.
4. Develop study-specific materials such as monitoring plans and training documents.
5. Oversee vendor activities like laboratory services and equipment provisioning.
6. Contribute to study-level forecasting, manage enrolment estimates, and reconcile across countries.
7. Monitor study timelines, deliverables, and budgets; provide updates and seek approval for budget deviations.

Requirements:

• Bachelor’s degree in healthcare or a related scientific field.
• Clinical monitoring experience required.
• 2-3 years of leading local, regional, or global teams.
• 2-3 years of clinical trial project management experience.
• Knowledge of clinical trial processes, operations, and ICH/GCP guidelines.
• Experience in project and program management, including budgets and timelines.

At IQVIA, we value camaraderie and professional growth, offering unique opportunities to advance your career alongside talented colleagues.

What We Offer:

• Opportunity to work on innovative medicines at the forefront of development.
• Access to extensive data pools for better site selection and recruitment, enhancing efficiency and productivity.
• Genuine career development opportunities within the organization.

#LI-REMOTE

IQVIA is a leading global provider of analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to pushing the boundaries of human and data science to make a meaningful impact—helping create a healthier world. Learn more at our website.