Clinical Research Associate II
On-siteSacramento, California, United States
Job Summary
Conduct ongoing study monitoring through 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. Generate clinical SOPs, policies, and plans adhering to US and international guidelines. Participate in protocol design, site evaluation, and study termination visits to obtain final reports for regulatory submission. Manage procurement of budgets, contracts, and regulatory documents while maintaining clinical archives. Requires BA, BS, RN, or BSN with 1-2 years of clinical research experience and GCP knowledge. Offers dental, medical, vision, 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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