Senior CRA: Global Trials & Impact (Travel 40–60%)

IQVIA; Bath; On-site; GBP 50,000 - 65,000; Full time

Job summary

IQVIA is seeking a Senior CRA to join the Clinical Functional Service Partnership (CFSP) team in the UK. The role involves on-site monitoring across sponsor programs, ensuring patient safety and data integrity, and collaborating with cross-functional study teams.

You will bring 2+ years of on-site monitoring experience, strong knowledge of GCP/ICH guidelines, and excellent communication to mentor junior staff and drive study timelines in a dynamic environment.

Qualifications

• University degree in Life Sciences or Health Sciences or related field.
• Minimum 2 years on-site monitoring experience in CRO/pharma/biotech.
• Strong knowledge of GCP, ICH guidelines and regulatory requirements.
• Experience in a sponsor-dedicated or CFSP environment preferred.
• Excellent communication and stakeholder management skills.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits per protocol and regulatory guidelines.
• Ensure sites maintain patient safety, data integrity, protocol compliance, and study quality.
• Build relationships with investigators and site personnel; provide coaching and support.
• Monitor progress, regulatory documentation, recruitment, data queries, and site performance metrics.
• Collaborate with cross-functional teams to support study delivery and timelines.
• Mentor junior team members through coaching and co-monitoring activities.
• Support study start-up, maintenance, close-out, and site financial activities as needed.

Skills

Life Sciences degree

GCP knowledge

ICH regulations

Excellent communication

Education

Bachelor's degree in Life Sciences

Job description

IQVIA is seeking a Senior CRA to join the Clinical Functional Service Partnership (CFSP) team in the UK. The role involves on-site monitoring across sponsor programs, ensuring patient safety and data integrity, and collaborating with cross-functional study teams.

You will bring 2+ years of on-site monitoring experience, strong knowledge of GCP/ICH guidelines, and excellent communication to mentor junior staff and drive study timelines in a dynamic environment.