Clinical Research Associate 1
On-siteRaleigh, West Virginia, United States
Job Summary
Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, and material handling procedures for assigned clinical trials. Assist in protocol design, generate clinical SOPs, and evaluate potential sites based on established criteria. Manage procurement of budgets, contracts, and regulatory documents while initiating studies through site visits and supply shipments. Prepare site visit reports, conduct termination visits, and maintain clinical archives. Requires BA/BS degree, GCP knowledge, and 1-2 years of clinical research experience. Join a team supporting US and international guidelines with full benefits including dental, medical, vision, PTO, and 401K.
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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