IQVIA

Clinical Research Associate 2, Sponsor Dedicated

IQVIA

full-time

Posted on:

Location Type: Remote

Location: Remote • California, Kansas, North Carolina • 🇺🇸 United States

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Salary

💰 $71,900 - $169,300 per year

Job Level

JuniorMid-Level

Tech Stack

Google Cloud Platform

About the role

  • Perform monitoring and site management work to ensure that sites are conducting the study(ies).
  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits).
  • Work with sites to adapt, drive and track subject recruitment plan.
  • Administer protocol and related study training to assigned sites.
  • Evaluate the quality and integrity of study site practices.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals.
  • Ensure copies/originals site documents are available for filing in the Trial Master File.
  • Create and maintain appropriate documentation regarding site management.
  • Collaborate and liaise with study team members for project execution support.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred.
  • Equivalent combination of education, training and experience may be accepted in lieu of degree.
  • Some organizations require completion of CRA training program or prior monitoring experience.
  • Basic knowledge of clinical research regulatory requirements (i.e., GCP and ICH guidelines).
  • Good therapeutic and protocol knowledge.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
  • Written and verbal communication skills including good command of English language.
  • Organizational and problem-solving skills.
  • Effective time and financial management skills.
  • Ability to establish and maintain effective working relationships.
Benefits
  • health insurance
  • retirement plans
  • paid time off
  • flexible work arrangements
  • professional development
  • bonuses

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
site monitoringsubject recruitmentregulatory submissionsstudy trainingdocumentation managementclinical researchGCPICH guidelines
Soft skills
communication skillsorganizational skillsproblem-solving skillstime managementfinancial managementrelationship building
Certifications
CRA training program