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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 running local studies across all therapeutic areas, managing the operational aspects of projects 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 other applicable local regulations.
Job Overview:
* Partner with global, local country teams, and study teams to provide high-level country strategy, drive study progress, and ensure country-level study delivery. (Accountable for study deliverables and key decisions within the country)
* Plan, manage, and oversee clinical study execution according to the global program strategy, leading the cross-functional Local Study Team (LST)
* Support country-level operational planning and be responsible for site selection within assigned countries
* Contribute to and develop program/study-specific materials such as monitoring plans and training documents
* Oversee and monitor vendor activities, e.g., laboratories and equipment provisioning
* Contribute to the study-level forecast for investigational products, support study accountability and reconciliation across countries, and manage enrollment long-range estimates (ELE)
* Monitor clinical study execution against timelines, deliverables, and budgets for each country
* Provide updates on study budgets and obtain approval for deviations outside the approved range
Requirements:
* Bachelor’s degree in healthcare or a related scientific discipline
* Clinical monitoring experience required
* At least 2-3 years’ experience leading local, regional, or global teams
* 2-3 years’ experience in clinical trial project management
* Knowledge of clinical trial processes and operations
* Extensive knowledge of ICH-GCP regulations and guidelines
* Experience in project and program management, including oversight of study deliverables, budgets, and timelines
* Understanding of time, cost, and quality metrics, and key performance indicators (KPIs)
Working at IQVIA offers unique opportunities for camaraderie and professional development, allowing you to advance your career 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 significant data pools for better 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 aim to push the boundaries of human and data science to make a significant impact—helping our customers create a healthier world. Learn more at IQVIA’s website.
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