Clinical Research Associate 1
On-siteDenver, Colorado, United States
Denver, Colorado, United StatesOn-siteFull TimeEntry LevelSmall
Full TimeEntry LevelSmall
Job Summary
Design and prepare clinical trial protocols, case report forms, and study initiation documents while generating standard operating procedures and policies per US and international guidelines. Evaluate potential clinical sites, procure budgets and regulatory documents, and conduct ongoing monitoring including site visits, protocol adherence checks, and file inspections. Prepare site visit reports, manage study termination visits, and maintain clinical archives. Requires BA/BS degree, GCP knowledge, and 1-2 years of clinical research experience. Dental, medical, vision, PTO, and 401K benefits included.
Required Qualifications
- BA, BS, RN, BSN or equivalent
- Basic knowledge and adherence to GCPs
- 1-2 years of clinical research experience or equivalent experience or training
- Strong attention to detail
- Ability to multi-task
- Unquestionable integrity and highest ethical standards
- Excellent written and verbal communication skills
- Self-motivated, assertive, and driven
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