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Senior Clinical Research Consortium Coordinator

Req # 34251 Job Location Los Angeles, California - US
The Clinical Research Consortium Coordinator, Sr. independently coordinates and manages all new approaches to Neuroblastoma Therapy (NANT) consortium activities at the coordinating center as it pertains to consortia protocols and clinical trials in conjunction with Consortium Administrator and Medical Director.  The Consortium Coordinator Sr. will be the main contact for all other participating sites to assist with all protocol related issues such as clarifications and compliance.  The individual must be detail oriented and have the ability to prioritize and handle multiple tasks/projects; must possess critical thinking skills and have the ability to analyze and troubleshoot issues as they arise.  Additionally, the individual must have interpersonal skills necessary to work effectively with external participating sites, ancillary staff & research team; must have great command of English language (professionally spoken &  written) must have excellent phone& e-mail etiquette; ability to work under pressure and have great attention to detail. As a Sr. Clinical Research Consortium Coordinator will  provide leadership for junior staff.

Minimum Qualifications / Work Experience:
·        5+ years of hospital based Phase 1-3 clinical trials experience with focus on Consortium related activities in Oncology.
·        At least 3 years of clinical trials data management experience
IDE/IND submission experience 

Bachelor’s Degree required, Masters preferred.

License, Registration or Certification Required: 
·        SoCRA or ACRP Certification is required within 6 months of hire

Strong computer skills with proficiency in Word, Excel, PowerPoint, etc.
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