CRA II: Oncology Trials & Compliance

AbbVie; Newport; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading global biopharmaceutical company is looking for a Clinical Research Associate in Newport, UK, to monitor clinical studies and ensure adherence to protocol and regulatory standards. You will conduct site visits, train personnel, and manage investigator agreements. The ideal candidate will have a tertiary qualification in health-related fields and extensive experience in Oncology, alongside strong analytical and organizational skills. Join us in making a significant impact on patients’ lives across key therapeutic areas.

Qualifications

• Extensive clinically-related experience in Oncology preferred.
• In-depth knowledge of regulations governing clinical research and ICH/GCP Guidelines.
• Strong planning and organizational skills in a dynamic environment.

Responsibilities

• Monitor activities conducted by clinical investigative sites for adherence.
• Conduct site qualification, initiation, interim monitoring, and study closeout visits.
• Train study site personnel on protocol and regulatory requirements.

Skills

Analytical skills

Organizational skills

Interpersonal skills

Communication skills

Education

Tertiary qualification in health-related field

Job description

A leading global biopharmaceutical company is looking for a Clinical Research Associate in Newport, UK, to monitor clinical studies and ensure adherence to protocol and regulatory standards. You will conduct site visits, train personnel, and manage investigator agreements. The ideal candidate will have a tertiary qualification in health-related fields and extensive experience in Oncology, alongside strong analytical and organizational skills. Join us in making a significant impact on patients’ lives across key therapeutic areas.