Clinical Research Associate

Lake Forest, IL, US • Posted 1 day ago • Updated 1 day ago
Contract W2
Contract Corp To Corp
On-site
Depends on Experience
Fitment

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Job Details

Skills

  • Auditing
  • Clinical Research
  • Collaboration
  • Communication
  • Documentation
  • Effective Communication
  • Evaluation

Summary

We are looking for Clinical Research Associate for our client in Lake Forest, IL
Job Title: Clinical Research Associate
Job Location: Lake Forest, IL
Job Type: Contract
Job Overview:
Pay Range: $40.16hr - $45.16hr

Responsibilities:

  • Assist senior staff with study planning and execution activities.
  • Support investigator site evaluation, selection, training, and ongoing management.
  • Coordinate and support study-related meetings and communications.
  • Prepare and assemble regulatory submissions in compliance with applicable standards.
  • Draft study protocols, reports, and supporting documentation.
  • Monitor investigational sites to ensure adherence to study protocols and regulatory requirements.
  • Ensure timely patient enrollment and track study progress.
  • Oversee Case Report Form (CRF) retrieval, processing, data cleanup, and classification.
  • Contribute to study summaries and reporting activities.
  • Act as a lead or mentor to junior CRAs when required.
  • Serve as the primary point of contact for investigational sites and ensure effective communication.
  • Collaborate with cross-functional study teams and management.
  • Support onboarding, training, and team integration through initial onsite presence.

Required Qualifications:

  • Bachelor s degree in Life Sciences.
  • 5+ years of clinical research monitoring experience, preferably at a Senior CRA level or ready for advancement.
  • Strong knowledge of ICH-Google Cloud Platform, FDA, and IRB regulations, including audit readiness.
  • Proven experience reviewing medical records and source documentation.
  • Demonstrated ability to independently monitor and manage clinical sites.
  • Strong cross-functional communication and stakeholder management skills.
  • Leadership experience, including mentoring junior CRAs and acting as Lead CRA across multiple studies and sites.

Preferred Qualifications:

  • Demonstrated career stability with consistent professional growth.
  • Experience in the In Vitro Diagnostics (IVD) therapeutic area.
  • Neurology clinical study experience.
  • Experience working with or within sponsor organizations.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10516350
  • Position Id: IL_CIRA_0414
  • Posted 1 day ago
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