About this role

Conducting and reporting all types of onsite monitoring visits
Driving the study startup phase (if applicable)
Performing CRF reviews, source document verification and query resolution
Be responsible for site communication and management
Supervising study activities, timelines, and schedules for each site
Acting as a point of contact for in-house support services and vendors
Supporting quality control, such as compliance monitoring and reports review
Participating in feasibility research
Supporting the regulatory team in preparing documents for study submissions and regulatory approval

BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
Independent on-site monitoring experience in the UK, ideally on multiple projects at a time
Demonstrable experience in all types of monitoring visits in Phase II and/or III
Strong written and verbal communication skills
Experience supporting Oncology studies is beneficial, but not essential
Intermediate to Advanced knowledge of MS Office
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills are essential
Full and clean driver's license, and the ability to travel

Clinical Research Associate II

Key skills