CRA II: Oncology Clinical Trials (UK)

IQVIA; Livingston; Presencial; GBP 30.000 - 42.000; Jornada completa

Descripción de la vacante

IQVIA Biotech is seeking an on-site Clinical Site Monitor to support oncology studies in the UK. You will conduct monitoring visits, ensure compliance with GCP/ICH, and liaise with sites to drive patient recruitment and data quality.

The role requires a Bachelor’s degree in a scientific field, 1–2 years of on-site monitoring experience, and strong English communication. UK right to work is required.

Formación

• GCP and ICH regulatory knowledge is required.
• Strong written and verbal English communication.
• Experience applying clinical trial requirements in practice.

Responsabilidades

• Perform site monitoring visits in line with GCP/ICH and contract scope.
• Work with sites to plan recruitment to support study timelines.
• Administer protocol training and maintain site communications.
• Evaluate site quality and ensure protocol/regulatory compliance.
• Track regulatory submissions, recruitment, CRF completion, and data queries.
• Maintain TMF/ISF documents per local requirements.
• Prepare visit reports and follow-up correspondence.

Conocimientos

On-site monitoring

Oncology studies experience

English communication

Educación

Bachelor's Degree in scientific discipline or health care

Descripción del empleo

IQVIA Biotech is seeking an on-site Clinical Site Monitor to support oncology studies in the UK. You will conduct monitoring visits, ensure compliance with GCP/ICH, and liaise with sites to drive patient recruitment and data quality.

The role requires a Bachelor’s degree in a scientific field, 1–2 years of on-site monitoring experience, and strong English communication. UK right to work is required.