Lead, Clinical Operations (Oncology Trials)

IQVIA Argentina; Reading; On-site; GBP 60,000 - 90,000; Full time

Job summary

IQVIA is seeking an experienced Clinical Operations Lead to support our sponsor-dedicated Clinical FSP team in the execution of complex clinical trials. The role involves coordinating with project teams, CROs and vendors to align study timelines and deliverables across multiple therapeutic areas.

The position emphasizes effective communication, feasibility assessment, site management and escalation as part of ensuring trial timelines are met and stakeholder expectations are fulfilled.

Qualifications

• 3+ years in biopharmaceutical or clinical research
• 1+ year in Clinical Project Management
• Oncology experience
• Bachelor’s degree in Science or related field
• Experience in multinational/global trials
• Strong vendor management experience
• Working knowledge of ICH-GCP and regulations
• Ability to manage multiple priorities across protocols

Responsibilities

• Assist in review, development and writing of trial documents and manuals
• Create Master ICF template and review site changes
• Participate in feasibility and evaluation of investigative sites
• Develop and manage study timelines and recruitment tools/retention plans
• Plan meetings with team support (investigator/coordinator meetings)
• Assist in IP and co-medication strategy development
• Monitor timelines and deliverables; manage vendors (monitoring, sample management, IVRS, lab)
• Develop relationships with investigational sites to enhance trial conduct
• Act as preliminary liaison for study sites to convey trial information and escalate as needed

Skills

Biopharma experience

Clinical project management

Oncology knowledge

Multinational trials experience

Vendors management

ICH-GCP knowledge

Communication skills

Prior coordination across teams

Education

Bachelor's degree in science

Tools

Vendor management

Job description

IQVIA is seeking an experienced Clinical Operations Lead to support our sponsor-dedicated Clinical FSP team in the execution of complex clinical trials. The role involves coordinating with project teams, CROs and vendors to align study timelines and deliverables across multiple therapeutic areas.

The position emphasizes effective communication, feasibility assessment, site management and escalation as part of ensuring trial timelines are met and stakeholder expectations are fulfilled.