Clinical Research Associate 1
On-siteNew Brunswick, Canada
Job Summary
Conduct ongoing study monitoring through frequent periodic site visits, protocol adherence checks, and inspection of study files for assigned clinical trials. Initiate studies by performing site visits, arranging shipment of clinical supplies and case report forms, and procuring budgets, contracts, and regulatory documents. Assist in protocol and case report form design, generate clinical SOPs, evaluate potential sites, and prepare site visit reports detailing key accomplishments and follow-up actions. Conduct study termination visits, obtain final reports from investigators, and maintain clinical archives and electronic files. Requires 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
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