ICF Reviewer II
PharmaCROClinical ResearchRegulatory AffairsQuality Assurancegcpemafdainform
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 .
Stand out for this role
NoxPharm tailors your CV to this job description by aligning your experience with the role requirements and terminology. Built for pharma & life sciences.
Tailor my CV now — free to trySimilar Pharma jobs
Senior Scientist I - Automation Engineer
Lonza — CN - Nansha
Senior Scientist I - Robotic Engineer
Lonza — CN - Nansha
Statutory Accounts & Tax Reporting Manager
Lonza — UK - Manchester
Senior Manufacturing Associate II (Principal Biotechnologist) – Large Scale Allogeneic - Day Shift
Lonza — US - Portsmouth, NH
Quality Control Specialist
Lonza — US - Portsmouth, NH
Specialist za podatkovno znanost in UI / Specialist Data Science & AI
Novartis — Ljubljana