As a key player in our team, you’ll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare
Job Summary
As a key player in our team, you’ll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare.
With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.
Matching Summary
As a key player in our team, you’ll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare.
Skills & Requirements
Must-have
site selection to close-out
develop and implement recruitment strategies
provide essential training and communication
evaluate and enhance site practices
monitor study progress
master meticulous documentation
manage site financials
Nice-to-have
drive innovation and excellence
groundbreaking advancements in healthcare
gain experience in therapeutic areas
collaborate with passionate team
Key Requirements
4 years on-site monitoring experience
preference for oncology trials
preference for haematology
strong knowledge of GCP
strong knowledge of ICH guidelines
Bachelor’s degree in scientific or healthcare discipline