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    FO

    Fortrea

    Clinical Research

    ICF Reviewer II

    Bucharest, RomaniaRemoteFull-time2+ yrs experiencePosted 1w ago
    All Fortrea jobs

    Job description

    Job Overview:

    Document Review Specialist I is responsible for reviewing Informed Consent Forms and Advertisements following project and country specific regulations as well as ICH-GCP, FDA and other regional guidance. Document Review Specialist I may responsible for reviewing revised protocols and core ICF’s.

      Summary of Responsibilities:

      • Review Country/Site Informed Consent Form to assure compliance with sponsor requirements, local regulatory requirements, and Good Clinical Practice (GCP) guidelines.
      • Review Patient Recruiting materials (Advertisements) to assure compliance with sponsor requirements, local regulatory requirements, and Good Clinical Practice (GCP) guidelines.
      • File Informed Consent Form, Patient Recruiting materials, and Investigator Package approval documentation in TMF and eTMF.
      • Review protocol amendment to reconfirm completeness and to assure compliance with Good Clinical Practice (GCP) guidelines.
      • Review revised Core Informed Consent Forms to reconfirm compliance with sponsor requirements, local regulatory requirements, and Good Clinical Practice (GCP) guidelines.
      • Provide input for Corrective and Preventative Actions (CAPAs) related to Document Review activities including Informed Consent Form Review, Patient Recruiting material Review and Investigator Package Review.
      • And all other duties as needed or assigned.

      Qualifications (Minimum Required):

      • University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology)
      • Fortrea may consider relevant and equivalent experience in lieu of educational requirements

      Experience (Minimum Required):

      • Working knowledge of ICH, FDA, IRB/IEC and other applicable regulations/guidelines.
      • 2 years’ work experience in clinical research
      • Previous interaction with operational project teams preferred.

      Preferred Qualifications Include:

      • Computer proficiency in MS Office (Word, Excel, PowerPoint, Access, Outlook e-mail and internet services)
      • Good written and oral communication skills
      • Well-developed organizational skills
      • Excellent proof-reading skills
      • Good time management skills with ability to consistently prioritize workload to accommodate multiple tasks and projects
      • Ability to work independently within a flexible team environment
      • Accuracy and Attention to detail
      • Analytical and problem-solving skills

      Physical Demands/Work Environment:

      • Standard office environment.

      Learn more about our EEO & Accommodations request here.

      Job details are sourced from the employer's original posting.

      Open job posting
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      About the company

      Fortrea

      Fortrea is a company that provides clinical trial and research services.

      View all Fortrea jobs
      Industry
      Clinical Research
      Open roles
      215

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