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.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
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 visits
Develop recruitment strategies
Empower sites with knowledge
Champion quality and integrity
Drive study progress
Master documentation
Manage site financials
Nice-to-have
Collaborate with passionate team
Gain experience in therapeutic areas
World-class training and mentoring
Key Requirements
At least 4 years on-site monitoring experience
Preference for oncology trials
Preference for haematology trials
Strong knowledge of GCP
Strong knowledge of ICH guidelines
Bachelor’s degree in scientific or healthcare discipline