• Clinical Research Associate (CRA) (all levels)

   

  Are you a passionate and dedicated Clinical Research professional looking to make a significant impact in the field of medical science? Join our client’s dynamic team as a Clinical Research Associate (CRA) and contribute to groundbreaking research based in either Chicago or Boston.

   

  Job Specifications:

  • Job Type: Full-Time
    

  • Location: Remote, based in Chicago or Boston
    

  • Pay Rate: Based on experience, Starting at $100,000
    

  • Travel: Up tp 80%
    

   

  Job Summary:

  As a Clinical Research Associate (CRA), you will play a crucial role in the planning, execution, and monitoring of clinical trials. You will ensure compliance with regulatory requirements, maintain high standards of data integrity, and work closely with investigative sites to facilitate successful study outcomes.

   

  Roles and Responsibilities:

  • Monitor clinical trials to ensure compliance with the protocol, regulatory requirements, and good clinical practice (GCP).
    

  • Conduct site visits, including pre-study, initiation, routine monitoring, and close-out visits.
    

  • Review and verify case report forms and other clinical data for accuracy and completeness.
    

  • Ensure proper documentation and reporting of adverse events.
    

  • Collaborate with clinical investigators and site staff to resolve issues and ensure timely data collection and reporting.
    

  • Prepare and present detailed monitoring reports.
    

  • Assist in the development and review of study-related documents, including protocols and informed consent forms.
    

  • Maintain up-to-date knowledge of regulatory requirements and industry best practices.
    

   

  Qualifications & Skills:

  • Bachelor’s degree in a related field (life sciences, nursing, pharmacy, etc.).
    

  • Minimum of 2 years of experience in clinical research or related field.
    

  • Strong knowledge of GCP, ICH guidelines, and FDA regulations.
    

  • Excellent organizational and communication skills.
    

  • Ability to work independently and manage multiple priorities.
    

  • Proficiency in Microsoft Office Suite and clinical trial management systems (CTMS).
    

   

  Opportunities:

  • Career advancement within a rapidly growing organization.
    

  • Professional development and continuous learning opportunities.
    

  • Participation in high-impact clinical trials and innovative research projects.
    

  • Networking with industry leaders and experts.
    

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