Regulatory Publishing Associate or Specialist

at  Novartis

SUMMARY

Our Regulatory Operations Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives. To do this, we are simplifying and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines to patients even faster. We are seeking key talent, like you, to join us in evolving the future of Regulatory Operations and give our patients and their families a brighter future to look forward to. Apply today and welcome to where we thrive together! The Role: This role offers hybrid working, requiring 3 days per week in our White City, London office. As a Global Regulatory Submission Publishing Associate or Specialist, you will be accountable for all clinical and submission publishing, verification, dispatch and coordination of HA compliant, worldwide regulatory submissions in support of Novartis global product portfolios.

MAJOR ACCOUNTABILITIES:

• Accountable for electronic preparation and publishing of quality reviews.
• Validate and dispatch clinical deliverables and global regulatory submissions.
• Produce high quality, clinical deliverables and global submissons to agreed timelines in compliance with worldwide HA requirements, internal working practices and guidelines.
• Act in a global capacity, and partner with various cross-functional stakeholders (e.g., Regulatory Affair Managers, Regulatory CMC Managers, Nonclinical Managers, Safety and Quality associates) as well as with Clinical Submission Managers, RA Operations Submission Managers and a publishing team located in multiple regions (e.g., US, EU, UK and India)
• Support the implementation of new technology, tools and processes, contribute to ongoing initiatives and training, and help identify continuous improvement opportunities.
• Support submission resource planning activities, as required

YOUR EXPERIENCE:

• Bachelor’s degree in life sciences or relevant discipline.
• Clinical and Global Submission publishing experience in the pharmaceutical or related industry.
• Experience in global regulatory submission formats including clinical deliverables
• Familiar with electronic clinical document publishing standards/formats, electronic and global (submission publishing standards/formats (e.g. eCTD, EU CTR)
• Working knowledge of publishing tools (e.g, DXC, Veeva), global submission validation tools, Document Management systems, Toolbox, HA electronic submission gateways, IRIS, CTIS, MS Office tools
• Familiarity with global Clinical and Regulatory HA requirements (.g. FDA, ICH, EMA, MENA region, CH, MHRA)
• Strong interpersonal and project management skills, and experience working in a complex, global cross functional organization.
• Highly motivated, organized and detailed oriented team player
• Ability to readily adjust to change in a fast-paced environment
• Positive attitude and ability to effectively collaborate with peers, stakeholders, cross-functional colleagues in a global team environment
• Fluency in English.
  Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?: https://www.novartis.com/about/strategy/people-and-culture
  Commitment to Diversity & Inclusion:
  Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.