Clinical Trial Operations Coordinator
1 month ago
The Coordinator, Clinical Trial Operations (CTO) plays a pivotal role in managing multi-center clinical and research studies. This individual must possess a broad spectrum of knowledge and experience in conducting clinical trials, with the ability to work independently and coordinate consortium activities at the central operations center.
The CTO will serve as the primary contact for consortium participating sites, ensuring seamless communication and collaboration. Key responsibilities include regulatory compliance, eCRF database configuration, system access management, and operational requirements. The ideal candidate will be detail-oriented, able to prioritize tasks, and possess excellent interpersonal skills to effectively work with external sites, research teams, and ancillary staff.
Minimum Qualifications- Minimum of 4 years of experience in Phase I-III clinical trials, with a focus on multi-center trials in oncology
- Clinical trial experience includes study protocol development, regulatory maintenance, and reporting, as well as eCRF development, data management, and coordination of investigational product
- IDE/IND submission experience is preferred
- Bachelor's Degree required (RN Degree is preferred), with a Master's Degree preferred
- SoCRA or ACRP Certification is required within 6 months of hire
- Strong computer skills with proficiency in Word, Excel, PowerPoint, and other relevant software
CHLA offers a competitive compensation package, with a pay scale ranging from $55,120.00 to $99,341.00. Final determination of a successful candidate's starting pay will be based on education and experience within the job or industry.
Additional pay may be determined for candidates who exceed the specified qualifications and requirements. CHLA provides a robust benefits program to meet the needs of its team members.
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