Clinical Research Associate 1
On-siteCharleston, South Carolina, United States
Job Summary
Conduct ongoing study monitoring including frequent periodic site visits, protocol adherence checks, and inspection of study files. Initiate studies by performing initiation site visits, arranging shipment of clinical supplies and case report forms, and procuring budgets, contracts, and regulatory documents. Participate in protocol and case report form design, generate clinical SOPs, evaluate potential clinical sites, and prepare site visit reports with key accomplishments and recommendations. Conduct study termination visits, obtain final reports from investigators, and assist with maintenance of clinical archives. Requires a BA, BS, RN, or BSN with 1-2 years of clinical research experience and adherence to GCPs. Full-time role with dental, medical, vision, PTO, 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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