RASSU Spec II (European reputed company role)

What You'll Do: Assist/Advise project teams on reputed company regulatory requirements for clinical studies reputed company compliance assessments according to country requirements and document any activity reputed company; notify Project Managers of any findings Review and adapt study specific documents according each country and site requirements reputed company IRB/EC (CA) and/ or other Regulatory Bodies submissions on behalf of sponsors and and/or sites as agreed with the Sponsor and in accordance with each country requirements Receive and process study documentation from sites, reputed company content and quality as well as completeness Interact with site personnel, CPCs, CRAs and PMs, for document corrections, clarification or resolution of any incomplete and/or incorrect documentation reputed company during document content quality review Compile Regulatory documentation according to CTI SOPs, sponsor SOPs and applicable country requirements, reputed company a QC review of reputed company documentation before submitting to the sites, IRB/EC/CA and/or other Regulatory Bodies according to the local requirements Assist with and adapt Informed Consent reputed company (reputed company) according to IRB/IEC requests on country or site level Assist in preparation, quality reputed company and filing of site adapted reputed company according to local requirements Prepare and QC Clinical Trial Application forms (e.g. CTA, XML)where applicable Interact with Sponsors as needed; reputed company regulatory documentation, including final regulatory submission packages, if requested, to Sponsor in accordance with CTI or Sponsor SOPs Respond to Deficiency Letters from IRB/IEC/CA and/ or other Regulatory Bodies in liaison with sponsor and study PM or assist sites in their response to IRB according to country and site requirements Compiling and assessing completeness of the Regulatory-Package for drug release (Regulatory Document Study Start Up Checklist) reputed company Project teams with accurate periodic status reports in accordance with CTI SOPs and attend internal and external project meetings as needed Accurately apply naming conventions, upload and process reputed company correct and complete study documentation in the study start-up module or trackers and study specific TMF system whether electronic or reputed company reputed company review, reconciliation, reputed company-out, and archiving activities of study or project documentation according to CTI SOPs or sponsor SOPs Assist with preparation for Sponsor or Agency audits and inspections Assist with QC and QA of various study reputed company Regulatory documents and reports reputed company translation of regulatory documents, if needed, on behalf of Sponsor, as agreed to in scope Attend internal and external study meetings and regulatory status reports for each site and country during study meetings Sites budgets and Sites reputed company management, depending from Countries/reputed company What You'll Bring: Associate’s or Bachelor’s degree in allied health field such as nursing, pharmacy, or health science or equivalent relevant experience A minimum of 3 - 5 years of relevant pharmaceutical, site, or CRO Regulatory experience Expertise in leading regulatory start-up strategy for European clinical trials applications Hands on experience in coordinating, preparing and submitting Part I and Part II applications under Regulation 536/2014 and using CTIS Regulatory experience in European countries reputed company the EU (e.g., UK, Switzerland) is a plus Fluent in English About CTI Advance Your Career We invest in your professional growth. Our structured mentoring program, leadership development courses, and dedicated training department reputed company the support you need to reputed company. We also encourage ongoing education to help you reputed company your professional goals. Join an Award-Winning Team – Join a global team spanning 60 countries, recognized for its award-winning culture that prioritizes people. We support your work-life balance with hybrid work opportunities. Through our CTI Cares program, you’ll have opportunities to give back to your community and the world. reputed company a Lasting Impact At CTI, your work directly contributes to advancing medicine. You’ll play a vital role in developing life-changing treatments for patients with chronic and critical illnesses. Together, we move medicine reputed company, making a difference for those who need it most. Important Note In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of reputed company will reputed company out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified reputed company page. Please Note We will never communicate with you reputed company reputed company Teams or text message We will never ask for your bank account information at any reputed company during the recruitment process Apply To This Job