With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of this data. We're on a mission to combine our next-generation sequencing and structured clinical data analytics capabilities with an innovative clinical trials network model to accelerate the pace of oncology research.  

 

Do you find the slow pace of drug development unacceptable? Are you ready to use cutting-edge technology to accelerate the completion of cancer clinical trials?  Are you passionate about improving patient access to new treatment options? We are looking for an experienced Clinical Research Coordinator, possessing innovative ideas and a desire to put them into action.

 

What you’ll do

  • Liaise with internal operations and industry/clinical research leaders 
  • Populate and review clinical trial budgets
  • Track study start-up milestones
  • Coordinate IRB submission with sponsors 
  • Support team members with the administrative tasks of the study (set up meetings, meeting notes, action item tracking)

 

Requirements

  • Bachelor’s Degree in a life science, or other related field
  • Minimum of three (3) years experience in working with complex clinical trials (site, sponsor or CRO)
  • Knowledge of FDA regulations, GCP, study start-up, clinical trial agreements, trial budgets, IRB submission and site operations
  • Excellent written and verbal communication skills
  • Excellent organizational and time management skills
  • Experience in a team environment
  • Ability to prioritize in a fast-paced environment
  • Working knowledge of Microsoft Office

 

Preferred Qualifications

  • Oncology experience
  • Experience with rapid site activation

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