Clinical Research Associate 1
On-siteAtlanta, Georgia, United States
Job Summary
Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, 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 design, site evaluation, and study termination visits to obtain final reports for regulatory submission. Generate clinical SOPs, policies, and plans adhering to US and international guidelines while maintaining clinical archives. Requires BA, BS, RN, BSN, or equivalent 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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