EU CTR Submission Lead job opportunity at Biogen Inc..



DateMore Than 30 Days Ago bot
Biogen Inc. EU CTR Submission Lead
Experience: 5-years
Pattern: full-time
apply Apply Now
Salary:
Status:

Job

Copy Link Report
degreeOND
loacation Warsaw, Poland, Poland
loacation Warsaw, Poland....Poland

About this role The EU CTR Submission Lead is responsible for leading and overseeing the full lifecycle of regulatory submissions for clinical trials conducted under the EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). This role provides strategic submission planning, cross-functional coordination, and subject matter expertise (SME) while ensuring timely, high-quality control, and compliant submissions across the EU/EEA. The Submission Lead is a senior technical leadership role, who plays a pivotal role in mentoring junior team members without direct line management responsibilities. Key Responsibilities 1. Regulatory Submission Leadership Lead planning and execution of Initial CTAs, Part I & II submissions, Substantial Modifications (SMs), and all CTIS lifecycle activities. Oversee preparation and submission of Requests for Information (RFIs), ensuring high-quality and timely responses. Provide subject matter expertise for end-of-study activities, including End-of-Trial (EoT) notifications, Summary of Results, Lay Summary, CSR and CSRr submissions. Conduct quality oversight and ensure alignment with EU CTR, EMA guidance, and internal standards operating procedures. 2. Strategic & Cross-Functional Leadership Serve as SME for EU CTR and CTIS processes, interpreting regulatory expectations. Lead submission readiness activities and coordinate with internal stakeholders (Regulatory Affairs, Clinical Trial Delivery and Clinical Trial Acceleration Units, Country & site Operations and Safety). Lead EU CTR Study Submission Team meetings to align submission strategy and timelines. 3. Compliance & Quality Oversight Ensure submissions adhere to EU CTR 536/2014, ICH-GCP, EMA guidance, and national requirements. Support audits and inspections related to submission activities. Contribute to development and maintenance of SOPs, work instructions, and templates. 4. CTIS System Expertise Lead complex CTIS activities: dossier creation, document upload, metadata accuracy, lifecycle management, public disclosure settings. Troubleshoot system issues and liaise with EMA as needed. Train project teams and stakeholders on CTIS functionalities and updates. Qualifications & Experience Bachelor’s or Master’s in Life Sciences or related field. 5+ years’ experience with EU CTR submissions and advanced CTIS expertise. Strong understanding of EU CTR timelines, dossier content, and results reporting. Proven ability to lead complex submission programs. Excellent communication, prioritization, and problem-solving skills. Experience in pharma, biotech, or CRO. Knowledge of regulatory intelligence and EU regulatory strategy. Core Competencies & Skills Strategic thinking Cross-functional leadership Problem-solving and analytical skills High attention to detail Excellent communication Please note that this role requires a candidate to be a holder of work permit & residency in Poland. About Biogen Poland Our Warsaw office is a complex hub for local, regional and global roles. Regardless our role and reporting line we’re driven every day by our unique purpose, working passionately to change the lives of patients affected by rare and devastating diseases. This is what gives us pride, inspires us and gives us fuel to push the boundaries of innovation. We represent over 30 nationalities and celebrate the strength that comes from differences in backgrounds, experiences, and perspectives. This commitment to fostering a supportive and inclusive workplace earned us a Great Place to Work Certificate and Best Places to Work Awards consecutively since 2021 in Poland and Europe. If our mission resonates with your heart and career aspirations, we’re inviting you to join our team. About Global Business Services (GBS) The Global Business Services (GBS) team transforms Biogen’s business processes, scaling global operations and fueling commercial growth and innovation. GBS adds value by delivering business solutions and support services through a global delivery model, operational transparency, and best practices. Aiming to be a world-class organization, GBS excels in people, solutions, execution, and partnerships, championing a continuous improvement culture recognized across Biogen. We form a great team of individuals with drive for innovation but also team players collaborating in the spirit of respect. And if you want to take your professional development in your own hands, this is a place for you. We give you a lot of opportunities for growth on a business and social ground.  #LI-Hybrid   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.

Other Ai Matches

Director, Search and Evaluation New Areas Applicants are expected to have a solid experience in handling Search and Evaluation New Areas related tasks
Head of Digital Transformation, Strategy, Patient Support Services Applicants are expected to have a solid experience in handling Strategy, Patient Support Services related tasks
Engineer III, Automation Applicants are expected to have a solid experience in handling Automation related tasks
Co-op, Materials Planning & Supply Chain Applicants are expected to have a solid experience in handling Materials Planning & Supply Chain related tasks
Co-op, Analytical Development Biologics Applicants are expected to have a solid experience in handling Analytical Development Biologics related tasks
Senior Medical Director, Global Medical Device Applicants are expected to have a solid experience in handling Global Medical Device related tasks
remote-jobserver Remote
Intern, Global Supply Planning Applicants are expected to have a solid experience in handling Global Supply Planning related tasks
Sr. Manager, Global Regulatory Affairs- West Coast Hub Applicants are expected to have a solid experience in handling Global Regulatory Affairs- West Coast Hub related tasks
(Senior) Product Manager, Taiwan, Hong Kong & Macau Applicants are expected to have a solid experience in handling Taiwan, Hong Kong & Macau related tasks
Associate Director, Data Science Lead Applicants are expected to have a solid experience in handling Data Science Lead related tasks
Executive Assistant to Heads of Clinical Development Applicants are expected to have a solid experience in handling Job related tasks
External Stakeholder Engagement (ESE) Sr Analyst – Portuguese Speaking Applicants are expected to have a solid experience in handling Job related tasks
Senior Manager, Global Pricing and Access Applicants are expected to have a solid experience in handling Global Pricing and Access related tasks
Medical Manager, NMD Applicants are expected to have a solid experience in handling NMD related tasks
remote-jobserver Remote
Clinical Development Lead, Rare Autoimmune Nephrology Programs Applicants are expected to have a solid experience in handling Rare Autoimmune Nephrology Programs related tasks
Global Commercialization Director, Lupus (CLE) Applicants are expected to have a solid experience in handling Lupus (CLE) related tasks
Key Account Manager, Rare Diseases FA (f/m/d) - area Essen, Wiesbaden, Kaiserslautern, Saarbücken, Aachen, Düsseldorf Applicants are expected to have a solid experience in handling Rare Diseases FA (f/m/d) - area Essen, Wiesbaden, Kaiserslautern, Saarbücken, Aachen, Düsseldorf related tasks
Product/Brand Legal Counsel - US Applicants are expected to have a solid experience in handling Job related tasks
Medical Director Global Medical Affairs, Epilepsy Applicants are expected to have a solid experience in handling Epilepsy related tasks
remote-jobserver Remote
Principal Medical Writer – GenAI and Regulatory Writing Innovation Applicants are expected to have a solid experience in handling Job related tasks
Global Commercialization Lead FA Applicants are expected to have a solid experience in handling Job related tasks
Director of Quality Control, Pharma Applicants are expected to have a solid experience in handling Pharma related tasks
Associate Director, Marketing - LUPUS Applicants are expected to have a solid experience in handling Marketing - LUPUS related tasks