Description
We are seeking a Regulatory Affairs Specialist to join our team in Buenos Aires. As a Regulatory Affairs Specialist, you will serve as the primary contact with investigative sites during study maintenance and site startup activities. You will be responsible for collecting required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within agreed timelines.
Summary of Responsibilities
- Develop awareness of regulatory legislation, guidance, and practice in assigned countries with senior staff support.
- Assist senior staff in compiling, preparing, submitting, and obtaining approval of submission documents to IRB/IEC/Third body/Regulatory Authority in accordance with local requirements.
- Liaise with internal and external vendors for Regulatory Authority submissions.
- Review final submission documents as applicable.
- Organize communication related to submissions/outcomes within Fortrea.
- Escalate study issues in a timely fashion.
- Perform other duties as assigned by management.
In Country Specific Tasks (Global)
- Serve as primary contact for investigative sites and collect required documents in a timely manner.
- Collect and track necessary documents, perform quality reviews, formatting, and compilation of final documents for site activation and maintenance.
- Ensure maintenance and start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality, and applicable laws.
- Update study documents when there are changes in study personnel/study amendments.
- Ensure high-quality documents are filed and systems are updated on an ongoing basis.
Clinical Trials Information System (CTIS) Tasks (Specific Centralized Role for EU)
- Upload submission documentation to CTIS under supervision.
Qualifications
- University/College degree (life science preferred) or certification in a related allied health profession.
- Relevant and equivalent experience may be considered in lieu of educational requirements.
Experience
- Minimum 0-2+ years of experience or an equivalent combination of education and experience.
- Working knowledge of ICH, RA, IRB/IEC, and other applicable regulations/guidelines.
- Basic understanding of the clinical trial process.
Physical Demands/Work Environment
- General Office Environment.