Project-based clinical research assistance

Does your clinical site have too many trials and not enough study coordinators?  Do your study coordinators or nurses need on-site training?  I offer site level clinical trial assistance to research centers, medical groups, and site maintenance organizations (SMOs).  If your site has a highly involved clinical trial, or if your site is short-staffed due to turnover or a leave of absence, my site level assistance can certainly come in handy. 

I can provide relief to your clinical research staff by:

  • Performing data entry tasks
  • Processing regulatory documents
  • Preparing for upcoming trials (i.e. creation of source documents)
  • Training staff members & SOP Writing

Site level assistance services

My services can be negotiated into your site contract with sponsors and clinical research organizations (CROs).  I can also be hired by a sponsor or CRO directly to provide extra site level assistance.  By investing in my services, you can ensure your site remains a top-performer, and you will always be prepared for a sponsor audit / FDA inspection.  Feel free to contact me to ask about ways I can help out your site.  My prices are very reasonable for site level assistance.  I can be hired on a contractual basis for both part-time and short-term assignments.

site level assistance

contact for site level assistance

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