Clinical Research Associate 1
On-siteNashville, Arkansas, United States
Job Summary
Design and prepare clinical protocols and case report forms while generating SOPs, policies, and plans adhering to US and international guidelines. Evaluate potential clinical sites, procure budgets and regulatory documents, and initiate studies by performing site visits and arranging clinical supply shipments. Conduct ongoing monitoring through periodic site visits, protocol adherence checks, and file inspections to prepare reports identifying key accomplishments and resolution issues. Execute study termination visits, obtain final investigator reports, and maintain clinical archives. Requires a BA, BS, RN, or BSN with 1-2 years of clinical research experience and GCP knowledge.
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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