IQVIA

Clinical Research Associate, Sponsor Dedicated

IQVIA

full-time

Posted on:

Location Type: Office

Location: Durham • California, Kansas, New Jersey, North Carolina • 🇺🇸 United States

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Salary

💰 $57,500 - $226,800 per year

Job Level

JuniorMid-Level

About the role

  • Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required.
  • Perform site monitoring visits in accordance with contracted scope of work and Good Clinical Practice.
  • 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.
  • 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.
  • Requires at least 2 years of on-site monitoring experience.
  • Equivalent combination of education, training and experience may be accepted in lieu of degree.
  • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
  • Good therapeutic and protocol knowledge as provided in company training.
  • 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 with coworkers, managers, and clients.
Benefits
  • Health insurance
  • Retirement plans
  • Paid time off
  • Flexible work arrangements
  • Professional development

Applicant Tracking System Keywords

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

Hard skills
site monitoringstudy managementregulatory submissionsclinical researchprotocol administrationdata reportingsubject recruitmentstudy trainingquality evaluationdocumentation management
Soft skills
communicationorganizational skillsproblem-solvingtime managementfinancial managementrelationship buildingcollaborationliaison skillsadaptabilityleadership