CRA II: Oncology Trials & Compliance

AbbVie; Kingswood; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading biopharmaceutical company located in Kingswood is seeking an experienced Clinical Research Associate to monitor clinical sites, ensuring compliance with protocols and regulations. The ideal candidate will have a health-related tertiary qualification, preferably with experience in oncology. Responsibilities include conducting site evaluations, training site personnel, and ensuring data quality throughout clinical trials. This role demands strong analytical and organizational skills, along with the ability to navigate dynamic project environments.

Qualifications

• Tertiary qualification in a health-related field preferred.
• Experience in clinical trials, especially in oncology.
• Understanding of ICH/GCP guidelines and regulations.

Responsibilities

• Monitor clinical investigative sites to ensure protocol adherence.
• Conduct site qualification, initiation, and closeout visits.
• Oversee site personnel's activities without direct authority.

Skills

Clinical research compliance

Oncology experience

Data quality assurance

Training site personnel

Negotiation skills

Education

Tertiary qualification in health-related field

Job description

A leading biopharmaceutical company located in Kingswood is seeking an experienced Clinical Research Associate to monitor clinical sites, ensuring compliance with protocols and regulations. The ideal candidate will have a health-related tertiary qualification, preferably with experience in oncology. Responsibilities include conducting site evaluations, training site personnel, and ensuring data quality throughout clinical trials. This role demands strong analytical and organizational skills, along with the ability to navigate dynamic project environments.