Clinical Research Associate

hace 6 horas


Xico, México Icon A tiempo completo
Study Start Up Associate

At ICON, we are committed to advancing clinical research and improving patient outcomes. As a Study Start Up Associate, you will play a critical role in ensuring the successful initiation of clinical trials.

Key Responsibilities:
  • Review and negotiate clinical site investigator contracts and budgets
  • Maintain communication with investigative sites, sponsors, and internal personnel regarding contract status and related documents
  • Prepare and oversee preparation of contractual documents and correspondence
  • Facilitate the indemnification process between the study sponsor and site
  • Develop and update training documentation and conduct group training as necessary
  • Mentor and train new and junior personnel in the study start up department
Study Start Up Associate (Regulatory Submissions)

As a member of the Study Start Up Team, you will be responsible for ensuring that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials.

  • Collect, prepare, review, approve, process, and track regulatory and site level critical documents required for study site activation
  • Competent Authority, Ethics Committee, and Institutional Review Board Submissions
  • Collect, review, organize, and assemble regulatory initial start-up and maintenance submission packages


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