Global Study Lead - Cross-Functional Delivery

IQVIA LLC; Reading; On-site; GBP 90,000 - 140,000; Full time

Job summary

IQVIA LLC in the United Kingdom seeks a Global Study Associate Director to lead cross-functional study teams within Study Management, BioPharmaceuticals Clinical Operations, delivering studies on time, within budget and to high quality standards.

The GSAD will act as the principal liaison between study teams and the Clinical Program Team, ensuring effective partnerships with internal and external stakeholders and maintaining inspection readiness.

Qualifications

• University degree in medical or biological sciences or related discipline.
• 5 years of relevant clinical experience in the pharmaceutical industry, including 2 years' project management experience.
• Extensive knowledge of ICH‑GCP, clinical research regulatory requirements and clinical study management processes.

Responsibilities

• Lead cross-functional study team and provide direction to enable successful study delivery.
• Oversee study progress against timelines, budget and quality standards; liaison with CPT and external partners.
• Ensure TMF completeness and readiness for audits in line with SOPs and ICH-GCP.

Skills

Cross-functional leadership

Project management

ICH-GCP knowledge

Strategic thinking

Communication skills

Team leadership

Education

University degree in medical/biological sciences

Tools

ACCORD/ABACUS

PharmaCM

Job description

IQVIA LLC in the United Kingdom seeks a Global Study Associate Director to lead cross-functional study teams within Study Management, BioPharmaceuticals Clinical Operations, delivering studies on time, within budget and to high quality standards.

The GSAD will act as the principal liaison between study teams and the Clinical Program Team, ensuring effective partnerships with internal and external stakeholders and maintaining inspection readiness.