Piedmont Healthcare

Clinical Research Associate

US, Blue Bell (ICON) · Contract

Work authorization requiredDetected 16 days ago

GCPAccessibilityClinical TrialsClinical ResearchResearchCollaboration

About the role

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Inclusion and Accessibility ICON is an equal opportunity employer.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Maintain up-to-date documentation in CTMS and eTMF systems
Support and track site staff training and maintain compliance records
Support subject recruitment and retention efforts at the site level
Resolve data queries and drive timely, high-quality data entry
Document site progress and escalate risks or issues to the clinical team
Collaborate with cross-functional partners including CTAs, LTMs, and CTMs
We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

A graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN

Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Visit our careers site to read more about the benefits ICON offers.

Clinical Research Associate - Early Development Multi Therapeutic - Regional (major hubs)
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

This listing is sourced directly from Piedmont Healthcare's careers page and normalized into a canonical job model.