The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice guidelines
Job Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice guidelines.
Candidates will work with sites to adapt recruitment plans, manage regulatory submissions, and ensure the integrity of study data.
IQVIA is recognized as a top workplace and seeks experienced professionals to accelerate innovation for a healthier world.
Matching Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice guidelines.
Skills & Requirements
Must-have
Independent on-site monitoring experience
Knowledge of GCP and ICH guidelines
Experience managing multiple clinical protocols
Ability to travel to diverse investigative sites
Nice-to-have
Oncology therapeutic area expertise
Strong communication with study teams
Proactive issue escalation skills
Key Requirements
Life science degree or equivalent industry experience
UK work authorization required (no visa sponsorship)
Demonstrated ability to manage multiple clinical trial protocols