Clinical Research Associate II
On-sitePhoenix, Arizona, United States
Job Summary
Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, and inspection of study files. Prepare site visit reports identifying key accomplishments, issues, and recommendations for follow-up actions. Participate in study initiation, site visits, and termination visits, while assisting in protocol design, SOP generation, and budget procurement. Manage clinical archives and electronic files under the direction of the clinical study team. Requires a BA, BS, RN, or BSN with one to two years of clinical research experience and adherence to GCPs. Offers dental, medical, vision, and 401K benefits.
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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