Global Clinical Trial Manager - Oncology & Vendor Lead

IQVIA; Reading; On-site; GBP 60,000 - 85,000; Full time

Job summary

IQVIA, Reading, is seeking aClinical Project Manager to oversee oncology trials across global sites. You will lead cross-functional teams, manage timelines and budgets, and ensure high-quality deliverables from initiation through study report.

The role requires strong ICH-GCP knowledge, vendor management experience, and the ability to handle multiple protocols and priorities in a fast-paced environment. UK-based candidates only; visa sponsorship is not available.

Qualifications

• 4+ years in the biopharmaceutical industry.
• 3+ years in Clinical Project Management at global level.
• Proven oncology therapeutic area experience.
• Bachelor’s degree or relevant science degree.
• Ability to manage multiple priorities across protocols.
• Strong vendor management experience.
• Working knowledge of ICH GCP and regulatory requirements.
• Experience executing trials from initiation to study report.
• Strong communication with teams, sites and vendors.

Responsibilities

• Deliver trials on time, within budget, and with high quality.
• Review, develop and write trial documents including protocols and CRFs.
• Lead site evaluation, selection, and feasibility.
• Coordinate and monitor vendors; review monitoring reports and co-monitoring visits.
• Develop and manage trial timelines, budgets, and priorities.
• Participate in data review and discrepancy resolution.
• Set up and maintain systems to plan and track trials.
• Generate management reports on trial conduct.
• Ensure recruitment, risk mitigation, and contingency plans.
• Lead multidisciplinary trial teams and study meetings.

Skills

Clinical Project Management

Oncology experience

Vendor management

ICH GCP knowledge

Global trials experience

Communication skills

Education

Bachelor’s Degree in Science

Job description

IQVIA, Reading, is seeking aClinical Project Manager to oversee oncology trials across global sites. You will lead cross-functional teams, manage timelines and budgets, and ensure high-quality deliverables from initiation through study report.

The role requires strong ICH-GCP knowledge, vendor management experience, and the ability to handle multiple protocols and priorities in a fast-paced environment. UK-based candidates only; visa sponsorship is not available.