EU CTR Submission Specialist

Position Summary

The EU CTR Submission Specialist is responsible for planning, preparing, managing, and maintaining regulatory submissions for clinical trials in compliance with EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). This role covers the entire lifecycle of a clinical trial, from initial application through substantial modifications to end-of-study reporting and public disclosure deliverables.

Key Responsibilities

1. Regulatory Submission Management

• Prepare, compile, and submit Initial Clinical Trial Applications (CTAs) in CTIS in line with EU CTR requirements.
• Coordinate and submit Part I and Part II documentation, ensuring compliance, accuracy, and consistency across EU/EEA Member States.
• Manage Substantial Modifications (SMs), safety notifications, administrative changes, and ongoing trial maintenance activities.
• Prepare, coordinate, and submit Requests for Information (RFIs) within mandated timelines.
• Execute all end-of-study regulatory activities, including End-of-Study (EoS) Notifications, submission of the Summary of Results and Clinical Study Report (CSR).
• Ensure all EU CTR-mandated reporting deadlines are met.
• Maintain accurate documentation in CTIS and internal tracking systems throughout the trial lifecycle.
• Monitor submission status and ensure proper lifecycle management.

2. Cross-Functional Collaboration

• Partner with Regulatory Affairs, Clinical Trial Acceleration and Clinical Trial Delivery units as well as Country and site operations.
• Provide guidance on CTIS processes and EU CTR obligations.
• Participate in EU CTR Study Submission Team meetings to align submission strategy and timelines.

3. Compliance & Quality Oversight

• Ensure compliance with EU CTR 536/2014, ICH-GCP, EMA guidance, and national requirements.
• Maintain awareness of CTIS updates and evolving regulatory expectations.
• Support inspections and audits.
• Ensure documentation quality, SOP adherence, and consistency.

4. CTIS System Expertise

• Manage operational tasks in CTIS including roles, dossier creation, uploads, and lifecycle management.
• Manage public disclosure settings and support redaction workflows.
• Troubleshoot CTIS issues and train internal teams.

Qualifications & Experience

• Bachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs, or related discipline.
• 1-3+ years of experience in EU clinical trial submissions or regulatory operations.
• Hands-on CTIS experience.
• Strong organizational and communication skills.
• Proficiency in English.
• Experience in pharmaceutical, biotech, or CRO environment.
• Proficiency with Microsoft Office applications and electronic document management systems.

Core Competencies & Skills

• Strong organizational skills, attention to detail, and ability to multitask effectively.
• Analytical and problem-solving skills, effective communication and can-do attitude
• Adaptability and ability to work under deadlines
• Understanding of regulatory frameworks

Job Level: Professional

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Client-provided location(s): Zug, Switzerland

Job ID: Biogen-REQ22224

Employment Type: FULL_TIME

Posted: 2026-01-09T19:11:59