Clinical Study Start Up Project Coordinator

Posted 1ds ago

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Job Description

Clinical Study Start Up Project Coordinator at Brown University Health developing and managing clinical documents. Collaborating with clinical teams to support research initiatives and maintain regulatory standards.

Responsibilities:

  • Review study protocols, consent forms, and manuals to extract relevant information to develop resources for the clinical team.
  • Develop and configure clinical research documentation.
  • Utilize study start up documents to initiate therapeutic EMR treatment plan creation.
  • Collaborate with Principal Investigator, clinical staff and pharmacy to gather requirements and ensure documentation and treatment plans meet clinical needs.
  • Create and distribute Letters of Collaboration with multiple departments as needed.
  • Troubleshoot and resolve issues related to clinical documents, treatment plans, and Letters of Collaboration.
  • Maintain all documentation dispersed to clinical team.
  • Participate in departmental meetings with regulatory and pharmacy.
  • Perform additional responsibilities as necessary.

Requirements:

  • Completion of a bachelor’s degree in relevant field
  • Strong understanding of clinical research workflow and protocol comprehension
  • Excellent written and verbal communication skills
  • Proficiency in Microsoft Office Suite
  • Exceptional attention to detail and organizational skills
  • Ability to work independently, manage multiple projects and meet deadlines.
  • Two years clinical research related experience preferred.