Clinical Project Manager

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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 drive healthcare forward!

As a Clinical Project Manager, you will be responsible for managing local studies across therapeutic areas, overseeing operational aspects to meet contractual requirements. You will act as the primary point of contact to lead, manage, and coordinate the conduct of clinical trials from study start-up (COLA) to close-out, in accordance with ICH-GCP and local regulations.

Job Overview:

• Partner with global and local study teams to develop country strategies, drive study progress, and ensure study delivery at the country level. You will be accountable for study deliverables and key decisions within your assigned country.
• Plan, manage, and oversee clinical study execution aligned with the global program strategy, leading the cross-functional Local Study Team (LST).
• Support operational planning at the country level and be responsible for site selection within your assigned countries.
• Contribute to the development of program and study-specific materials such as monitoring plans and training documents.
• Oversee vendor activities, including laboratories and equipment provisioning.
• Contribute to study-level forecasting for investigational products, support study accountability and reconciliation, and manage enrollment long-range estimates (ELE).
• Monitor study progress against timelines, deliverables, and budgets, providing updates and obtaining approvals for budget deviations outside the predefined range.

Requirements:

• Bachelor’s degree in healthcare or a related scientific discipline.
• Experience in clinical monitoring is required.
• At least 2-3 years of experience leading local, regional, or global teams.
• Minimum 2-3 years of clinical trial project management experience.
• Knowledge of clinical trial processes and operations.
• Extensive understanding of ICH-GCP regulations and guidelines.
• Experience in project and program management, including oversight of study deliverables, budgets, and timelines.
• Familiarity with time, cost, and quality metrics, and key performance indicators (KPIs).

At IQVIA, we offer opportunities for professional growth and development, working alongside diverse and talented colleagues.

What is in it for you?

• The opportunity to work on cutting-edge medicines at the forefront of new drug development.
• Access to extensive data pools to enhance site selection and recruitment, making the CPM role more efficient and productive.
• 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 advancing human and data sciences to create a healthier world. Learn more at our website.