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.
Skills Required
- University or college degree, preferably in life sciences, or certification in a related allied health profession
- Relevant and equivalent experience may substitute for educational requirements
- Working knowledge of ICH, FDA, IRB/IEC, and other applicable regulations and guidelines
- Two years of work experience in clinical research
- Previous interaction with operational project teams
- Proficiency with Microsoft Office, including Word, Excel, PowerPoint, Access, and Outlook
- Good written and oral communication skills
- Well-developed organizational skills
- Excellent proofreading skills
- Strong time management and prioritization skills
- Ability to work independently within a flexible team environment
- Accuracy and attention to detail
- Analytical and problem-solving skills
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.







