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Research (New Jersey)

available evenings
available overnight
available weekends
education completed: associates
license info: CCRP licensed by the (ACRP) Association of Certified Research Professionals

Certified Research Coordinator, looking for contract work part-time
Organized and can help with clinical study documentation (e.g. Main Study Files, CRFs, etc.) including preparation for internal/external audits, final reconciliation and archive. Ordering/dispatch and tracking of trial materials (e.g. binders, notebooks, lab supplies, drug supplies) as appropriate.
Familiar with ICH GCP, appropriate regulations, relevant SOP’s and internal tracking systems.
Reviewed Drug Accountability Forms for completion and communicated to central lab for release of study drug to approved sites.
Experience with coordinating duties associated with study initiation/closeout, investigators' and site personnel training, and site personnel credentialing.
Can contact clinical sites for specific requests (e.g., enrollment updates, missing documentation, etc.)
I have excellent references...
  • OK for recruiters to contact this job poster.
  • it's ok to contact this poster with services or other commercial interests

post id: 6981754585

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