Regulatory Professional managing clinical trial submissions in EU. Collaborating with teams across Europe optimizing processes and ensuring compliance.
Responsibilities
Working on process optimisation for CTA submissions within a team and stakeholders from other teams.
Working closely with various submission teams across the organization and all countries in Europe.
Managing initial clinical trial application submissions in the EU according to the Clinical Trial Regulation (EU CTR) and all changes during the life cycle of clinical trials.
Maintaining documents in the Clinical Trial Information System (CTIS) and ensuring accurate data about clinical trials.
Coordinating responses for requests for information from Health Authorities and Ethics Committees.
Ensuring timely submissions in CTIS and contributing to project team decisions.
Shaping the future setup of new processes for submitting Clinical Trial Applications (CTAs).
Collaborating with different IT platforms, such as Veeva Vault RIM and Vault Clinical (COSMOS).
Requirements
Master’s degree in life science or relevant field.
+ 5 years of experience in working with clinical trials and submissions.
EU Clinical Trial Regulation 536/2024 (EU CTR) understanding and experience.
Experience in working with Vault RIM and Vault Clinical (Veeva platforms), it’s a plus.
Experience working with Clinical Trial Information System (CTIS) (how to upload documents and knowledge of full CTIS structure for Part I and part II) – is a big advantage.
Fluency in written and spoken English.
Experience with improvement of workflows/optimisation projects.
Benefits
Opportunities to learn and develop
Health insurance
Retirement plans
Job title
Regulatory Professional – Clinical Trial Submissions, EU
Specialist in Regulatory Compliance supporting sustainability initiatives at FERI Group. Responsible for analysis, reporting, and development of sustainable finance products.
Export Control / Trade Compliance Officer ensuring customs compliance with Australian and U.S. laws. Advising on trade compliance issues and solutions across various projects and teams.
Graduate role in Internal Audit & GRC services at PwC, supporting organisations in regulatory compliance and risk management. Assisting with data analysis, process mapping, and client engagements.
Vice President of Compliance & Regulatory Affairs leading compliance strategy for Cotulla Education. Supporting growth and regulatory compliance across multiple institutions and campuses.
Compliance Officer with focus on AML and compliance tasks at Schulz & Cie. Consulting. Conducting audits, transaction monitoring, and managing regulatory issues in financial services.
Lead compliance and risk management at Thndr Securities Brokerage, ensuring regulatory adherence and overseeing compliance operations. Collaborate with teams to mitigate risks and educate on compliance programs.
Key contributor in Integrated Resource Planning at Duke Energy. Prepare executives for regulatory testimonies on future energy demands and regulatory compliance.
CMC Regulatory professional managing regulatory compliance activities for veterinary biological products at Zoetis. Supporting development and inspections for the new GMS Atlanta site with FDA and USDA expectations.
Compliance Associate supporting Fidelity's Asset Management Compliance operations through various responsibilities in financial services. Engaging in problem - solving and maintaining organizational compliance while collaborating with multiple departments.
CMC Regulatory professional at Zoetis preparing regulatory documentation and ensuring compliance with FDA and USDA regulations. Managing facility documents and participating in cross - functional project improvements.