Oncology Freelance CRA — Field Monitoring Expert

IQVIA LLC; East Boldon; On-site; GBP 42,000 - 64,000; Full time

Job summary

IQVIA LLC in the United Kingdom is seeking an experienced Clinical Research Associate to monitor Phase I–IV trials. You will perform site evaluations, initiation visits, and ongoing monitoring in line with Good Clinical Practices and IQVIA Biotech procedures, coordinating with the CTM or Lead CRA to ensure study requirements are met.

Responsibilities include investigator recruitment visits, training on eCRF/EDC, data quality reviews, and timely preparation of monitoring reports.

Qualifications

• Minimum of 2 years experience as a CRA.
• Experience in monitoring and/or coordinating clinical trials.
• Oncology experience required.
• Excellent written and verbal communication skills.
• Ability to form productive professional relationships both internally and externally.
• Ability to handle several priorities within multiple, complex trials.
• Able to work independently, prioritize, and work within a matrix team environment.
• Knowledge of current GCP/ICH guidelines.

Responsibilities

• Participates in investigator recruitment and site evaluation visits.
• Coordinate initiation activities and training on eCRF and EDC systems.
• Assists in resolving issues to ensure compliance with site file audits.
• Adheres to GCP/ICH guidelines and prepares monitoring reports.
• Documents accountability and storage conditions of trial materials.
• Reviews the quality and integrity of clinical data and resolves data queries.
• Reviews protocols, eCRFs, and study manuals as requested by CTM/Lead CRA.
• Serves as primary contact between IQVIA Biotech and investigators.
• Attends Investigator Meetings and study-related meetings.
• Ensures study deliverables are completed per timelines.
• Conducts Field Evaluation Visits and field training of CRAs.
• Maintains knowledge of all functional areas of clinical trials.

Skills

CRA experience

Clinical monitoring

Communication skills

GCP knowledge

Oncology experience

Job description

IQVIA LLC in the United Kingdom is seeking an experienced Clinical Research Associate to monitor Phase I–IV trials. You will perform site evaluations, initiation visits, and ongoing monitoring in line with Good Clinical Practices and IQVIA Biotech procedures, coordinating with the CTM or Lead CRA to ensure study requirements are met.

Responsibilities include investigator recruitment visits, training on eCRF/EDC, data quality reviews, and timely preparation of monitoring reports.