Summary

Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people's lives.

To do this, we are optimizing 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 and help give people with disease and their families a brighter future to look forward to.

Apply today and welcome to where we thrive together!

This role offers hybrid working, requiring 3 days a week / 12 days a month based in office.

As Senior Global Program Regulatory Manager, you will work with limited supervision to develop and implement the global regulatory strategy for program(s) through development, registration and post approval in the assigned region(s). You may act as the RA program lead on programs of limited complexity.

• Provide input to global program regulatory strategy, including regulatory designations & innovative approaches and may provide global RA leadership for specific part of the program or act as lead for a program of limited complexity.
• Coordinates regulatory readiness with other line functions, Country Organizations & Regions, representing RA or leads in regional RA or cross-functional activities providing strategic input into cross functional deliverables.
• Contributes to the development and maintenance of key documents, determines the requirements and coordinates the activity for HA interactions. May lead or serve in HA meetings or local HA liaison respectively.

• Leads planning, preparation and submission of clinic trails, and the implementation of defined global registration strategy into regional submissions worldwide with country organsiations.
• Coordinates, plans and prepares for submission of initial registrations and post approval applications, and the preparation, review and maintenance of local product information as assigned.
• Lead regulatory activities during HA reviews, responding to questions and HA interactions.

• Ensures timely RA input and submission of regulatory compliance and maintenance reports, maintaining regulatory information in compliance databases and document management systems.

• May serve as a RA subject matter expert and assume a mentoring role.

• You may also focus on one of the following key areas of activity:
  • Maintenance - preparation of selected global regulatory submissions.
  • Portfolio Transformation - e.g. streamlining activities, divestment/ integration, portfolio transformation and manufacturing transfer.
  • Business & Operational Excellence - collating, for example, registration samples, CPPs etc. to support submissions.

• Science based bachelors or advanced degree, plus advance understanding of pharmaceutical development, clinical trails.
• Awareness of post marketing/ brand optimization strategy, with track record of involvement in regulatory or pharmaceutical development in Phases I - IV, in multiple geographies.
• Strong interpersonal skills and experience working in a complex, cross functional organization and leading cross function teams.
• Compliance and Quality mindset.
• Fluency in English.