Clinical Research Associate 1
On-siteBleiblerville, Texas, United States
Job Summary
Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, and inspection of study files. Prepare site visit reports identifying key accomplishments, issues, and follow-up recommendations. Generate clinical SOPs, policies, and plans adhering to US and international guidelines while assisting in protocol and case report form design. Initiate studies by performing site visits, arranging shipment of supplies and forms, and procuring budgets, contracts, and regulatory documents. Conduct study termination visits to obtain final reports from investigators and participate in regulatory submission preparations. Maintain clinical archives and electronic files. Requires BA, BS, RN, or BSN; 1-2 years of clinical research experience; GCP knowledge; and strong attention to detail. Dental, Medical, Vision, PTO, and 401K benefits provided.
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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