Remote Oncology CRA – Clinical Trials Monitor

BeiGene; United Kingdom; On-site; GBP 40,000 - 50,000; Full time

Job summary

A global biopharmaceutical company is seeking a Clinical Research Associate to execute monitoring activities for oncology clinical trials in the UK. The role requires a minimum of 2 years of relevant experience, preferably in oncology trials. Responsibilities include ensuring compliance with ICH guidelines, managing site performance, and collaborating with clinical operations. Candidates should possess strong communication and organizational skills, along with proficiency in data analysis and various software tools.

Qualifications

• Minimum of 2 years of monitoring experience in clinical trials.
• Experience in oncology global trials preferred.
• Fluent in English (writing and speaking).

Responsibilities

• Execute clinical monitoring activities at clinical trial sites.
• Monitor trials in accordance with ICH guidelines and GCP.
• Collaborate with the Regional Clinical Operations Manager.

Skills

Monitoring experience

Communication skills

Organizational skills

Data analysis

Education

BS in a relevant scientific discipline

Tools

Microsoft Word

Microsoft Excel

MS Project

MS PowerPoint

Outlook

Job description

A global biopharmaceutical company is seeking a Clinical Research Associate to execute monitoring activities for oncology clinical trials in the UK. The role requires a minimum of 2 years of relevant experience, preferably in oncology trials. Responsibilities include ensuring compliance with ICH guidelines, managing site performance, and collaborating with clinical operations. Candidates should possess strong communication and organizational skills, along with proficiency in data analysis and various software tools.