Clinical Research Associate 1
On-siteOklahoma City, Oklahoma, United States
Job Summary
Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, and material handling procedures for assigned clinical trials. Participate in the design of protocols and case report forms, generate clinical SOPs, and evaluate potential clinical sites based on established criteria. Manage procurement of budgets, contracts, and regulatory documents, while initiating studies through site visits and arranging shipment of clinical supplies. Prepare site visit reports detailing key accomplishments and recommendations for follow-up actions, and conduct study termination visits to obtain final reports from investigators. Assist with the maintenance of clinical archive and electronic files. Requires a BA, BS, RN, or BSN with 1-2 years of clinical research experience and adherence to GCPs.
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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