Clinical Research Associate II
On-siteNew Orleans, Louisiana, United States
Job Summary
Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, and inspection of study files for assigned clinical trials. Participate in design and preparation of protocols, case report forms, and site visit reports while generating clinical SOPs, policies, and plans per US and international guidelines. Initiate studies by performing initiation site visits, arranging shipment of clinical supplies, and procuring budgets, contracts, and regulatory documents. Manage study termination visits, obtain final reports from investigators, and assist in maintaining clinical archives. 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
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.