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Associate Research Operations

Thousand Oaks, CA
“This Company requires all staff, staff augmentation external workers, and certain other external workers, in the United States and  puertricvaccinated from COVID 19 as a condition of assignment at this company. In accordance with applicable law, this company will provide reasonable accommodations staff augmentation external workers qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship this company, its operations, or its staff.”                                                        

Top 3 Must Have Skills                                                        
  • Strong attention to detail, including the ability to verify data/information, proofread and reformat documents
  • Experience in reading, understanding, and applying scientific data integrity checks to nonclinical research study reports, final study reports, and/or contributing scientist reports, and other regulatory documents
  • Knowledge of scientific/technical writing and editing

Day to Day Responsibilities:                
  • Ensure consistency and compliance with report writing and ELN documentation procedures
  • Conduct formal QC review and data verification of nonclinical research study reports, supporting ELNs, and other regulatory documents
  • Participate in the development and alignment of QC timelines for regulatory documents and preparation of assigned deliverables
  • May collaborate with external contractors and contracted research organization (CRO) vendors on QC related matters
  • Potential growth opportunity to train as a nonclinical study report coordinator (based upon performance and/or functional area need)

"This posting is for Contingent Worker, not an FTE"

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