Clinical Project Manager

TN United Kingdom; Cambridge; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Clinical Project Manager to join their dynamic team. This role offers the chance to lead local studies across various therapeutic areas while managing the operational aspects of clinical trials. As a key point of contact, you will ensure compliance with ICH-GCP regulations and drive study progress by collaborating with global and local teams. The position provides flexibility with remote, hybrid, or office-based working options, and the opportunity to work on cutting-edge medicines that significantly impact healthcare. If you are passionate about clinical research and want to advance your career, this is the perfect opportunity for you.

Benefits

Career development opportunities

Work on cutting-edge medicines

Access to significant data pools for better site selection

Qualifications

• 2-3 years of clinical trial project management experience required.
• Extensive knowledge of clinical trial processes and ICH/GCP regulations.

Responsibilities

• Manage local studies and operational aspects of projects to meet contractual requirements.
• Lead and coordinate clinical trials from start-up to close out.

Skills

Clinical monitoring

Project management

Knowledge of ICH/GCP regulations

Time, cost and quality metrics

Key performance indicators (KPIs)

Education

Bachelor’s degree in healthcare or scientific discipline

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 are growing, join us on our mission to drive healthcare forward!

As Clinical Project Manager, you will be responsible for running local studies in 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 co-ordinate 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:

1. Partner with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery. (Accountable for study deliverables and drives key decisions within set country)
2. Plan, manage, and maintain oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional Local Study Team (LST)
3. Support country-level operational planning and accountable for site selection within assigned country(ies)
4. Contribute and develop to program/study-specific materials – e.g., monitoring plan, study specific training documents.
5. Oversight and monitoring of applicable vendor activities e.g., laboratories and equipment provisioning.
6. Contribute to the study-level forecast for investigational product, support study level accountability and reconciliation across assigned countries, management of ELE (enrolment long-range estimates) process.
7. Monitor the execution of the clinical study against timelines, deliverables, and budget for that country:
8. Provide updates regarding the study budget and obtain approval for budget deviations for clinical sites (outside of range)

Requirements:

• Bachelor’s degree in a healthcare or other scientific discipline
• Clinical monitoring experience required.
• Minimum 2-3 years’ experience of leading local/regional or global teams
• Minimum 2-3 years’ clinical trial project management experience
• Clinical trial processes and operations
• Extensive knowledge of ICH/GCP regulations and guidelines
• Project and Program management including oversight of study deliverable, budgets and timelines.
• Time, cost and quality metrics, Key performance indicators (KPIs)

From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.

What is in it for you?

• The chance to work on cutting edge medicines at the forefront of new medicines development.
• IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CPM role more efficient and discussions at site more productive. Next generation clinical development!
• We offer genuine career development opportunities for those who want to grow as part of the organization.

#LI-REMOTE

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at