Associate Site Report Specialist

IQVIA Inc

Fully remote
Study monitoring plan drafting
Clinical trial supplies management
Global study performance dashboard development
Provide project related assistance for assigned project(s), sites and project teams, ensuring all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements

Job Summary

  • Provide project related assistance for assigned project(s), sites and project teams, ensuring all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements.
  • Develop, Prepare, & Maintain the Global study performance dashboard by acquiring data from primary or secondary data sources and assist the Study team in various phases by providing detail analysis of the data.
  • Assist with tracking and management of Case Report Forms (CRFs), queries and clinical data flow, and perform detailed quality checks of documents uploaded into the TMFs.

Matching Summary

Provide project related assistance for assigned project(s), sites and project teams, ensuring all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements.

Skills & Requirements

Must-have

  • study monitoring plan drafting
  • clinical trial supplies management
  • global study performance dashboard development
  • data analysis for trial mitigation
  • updating and maintaining system data
  • resolving data discrepancies
  • designing clinical and administrative reports

Nice-to-have

  • advocate compliance with SOPs
  • on the job training participation
  • quality improvement initiatives
  • collaboration with IT and clinical staff
  • systems expert guidance

Key Requirements

  • Bachelor's Degree in healthcare or scientific discipline
  • 3-5 years Clinical Research experience
  • Minimum 2 years on-site or remote monitoring experience
  • Equivalent combination of education, training and experience

Work Rights

Not specified

Tailored Resume

Cover Letter