About this role

You will be dedicated to a single client
You will be responsible for all site management and supervisory activities in the assigned oncology studies.
You will work with industry leaders and subject matter experts.
You will have the opportunity to mentor junior CRAs.
You will work with world-class technology.
You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.

Extensive experience in site management, with knowledge of clinical trial methodology and terminology.
Experience in oncology trials site monitoring, at least 4 years.
Minimum 4 years’ experience in independent site monitoring of all types of visits.
Effective time management, organizational and interpersonal skills and problem-solving skills, with the ability to multi-task and priorities.
Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research legislation and guidelines.

Senior Clinical Research Associate – Oncology

Key skills