Piedmont Healthcare
CRA II
Regional United States (PRA) · Mid · Contract
Sponsorship not specifiedDetected 12 days ago
GCPAccessibilityClinical TrialsClinical ResearchResearchCommunicationCollaboration
About the role
- 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.
Responsibilities
- Performing data review and resolution of queries to maintain high-quality clinical data.
- We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
Requirements
- Minimum of 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Ability to work independently and collaboratively in a fast-paced environment.
- Willingness to travel as required (approximately 60%)
Compensation
- Competitive base salary and performance related incentives
Benefits
- 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.
- Bachelor's degree in a scientific or healthcare-related field.
- Rewards & Benefits
- ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
- Benefits may include:
- Benefits may vary depending on role and location.
Equal opportunity
- ICON is an equal opportunity employer.
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This listing is sourced directly from Piedmont Healthcare's careers page and normalized into a canonical job model.