Clinical Trial Manager (Oncology)

Location: Reading, Berkshire, United Kingdom; only candidates based in the listed location will be considered.

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Manage clinical trial implementation, timelines, budgets, priorities, and feasibility activities.
• Lead investigative site evaluation and selection, patient recruitment planning, and risk-mitigation activities.
• Select, coordinate, and monitor vendors, including review of monitoring reports and co-monitoring visits.
• Support the development and review of protocols, case report forms, informed consent forms, clinical study reports, and regulatory documents.
• Coordinate data review, discrepancy resolution, study safety monitoring, quality metrics, and clinical trial supply plans.
• Lead multidisciplinary study teams, meetings, reporting, and training for CRAs and third-party vendors.

Requirements

• At least 4 years of experience in the biopharmaceutical industry.
• At least 3 years of global clinical project management experience.
• Professional experience and knowledge in oncology.
• Bachelor’s degree or another relevant degree with a strong science focus.
• Experience managing multiple protocols and therapeutic areas, vendors, and clinical trial activities from initiation through the clinical study report.
• Working knowledge of ICH Good Clinical Practices and other relevant regulatory requirements; English CV required.

Culture & Benefits

• Work closely with a sponsor-dedicated client project team.
• Opportunity to manage clinical research projects across different therapeutic areas.
• This role is not eligible for UK visa sponsorship.