Oncology Clinical Research Associate - Site Monitoring

IQVIA LLC; Horsforth; Sur place; GBP 30 000 - 50 000; Plein temps

Résumé du poste

IQVIA Biotech is recruiting for an on-site Monitoring role in the UK. You will conduct site visits for Oncology studies, ensure protocol adherence and regulatory compliance, and support recruitment plans.

You will train site personnel and maintain robust communication with investigators and the study team. The role requires at least 1 year of on-site monitoring experience, strong English communication, and solid knowledge of GCP/ICH guidelines.

Qualifications

• Minimum of 1 year of on-site monitoring experience.
• Experience monitoring Oncology studies is a must.
• Basic knowledge of GCP/ICH guidelines.
• Strong written and verbal English communication.
• Good organizational and problem-solving skills.

Responsabilités

• Perform site monitoring visits in compliance with GCP/ICH and contract scope.
• Drive and track subject recruitment plans to enhance predictability.
• Administer protocol training to sites and maintain communication.
• Manage site regulatory submissions and TMF/ISF documentation.
• Report monitoring findings and implement action plans.
• Collaborate with study team for project execution support.

Connaissances

On-site monitoring

Oncology studies

GCP/ICH knowledge

Communication skills

Time and financial management

English proficiency

Formation

Bachelor's Degree in a scientific discipline or health care

Outils

MS Word

MS Excel

PowerPoint

Description du poste

IQVIA Biotech is recruiting for an on-site Monitoring role in the UK. You will conduct site visits for Oncology studies, ensure protocol adherence and regulatory compliance, and support recruitment plans.

You will train site personnel and maintain robust communication with investigators and the study team. The role requires at least 1 year of on-site monitoring experience, strong English communication, and solid knowledge of GCP/ICH guidelines.