This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Ensure the appropriate conduct of clinical trials in line with the Study Monitoring Plan, relevant laws, and Good Clinical Practices.

• Oversee operational elements for executing clinical trial activities at designated investigator sites, from site activation to database lock.

• Collaborate with the study team to facilitate effective communication among team members and vendors.

• Monitor site-level Adverse Events (AEs) and Serious Adverse Events (SAEs), work closely with the Drug Safety Unit, and maintain follow-up with investigators.

⛳️ Requirements

• A Bachelor’s degree in life sciences or a professional degree in life sciences such as nursing, pharmacy, or a medical background, or equivalent qualifications.

• In-depth knowledge of clinical trial methodologies, ICH/GCP, FDA regulations, and local country laws.

• At least 3.5 years of relevant experience in clinical research site monitoring, preferably in the field of Oncology.