Management role with key responsibilities to inspire and lead a growing team of US regulatory experts with responsibility for ensuring excellent relationships with FDA and providing US regulatory expert strategy for a truly impactful family of products.
Position holder (PH) will have the following responsibilities within a specific GRA project/portfolio within GSK Vaccines:
• Managerial responsibilities for US-based staff within a specific portfolio, including resources overview and optimization at US GRA level, advice for US specific activities/processes, ensure appropriate training of US-based staff, and issue escalation
• Cross portfolio aligned regulatory strategy to assure timely approvals for all US submissions.
-Attend Head RA RDC staff meeting or RDC product strategy meetings and other relevant meetings as appropriate in agreement with RA RDC Head and NARA Head.
- Facilitate integration of US-based individuals within portfolio group and integration of US-specific regulatory aspects into projects in general within the portfolio
- Ensure US-specific regulatory learnings are shared with the rest of the team, in line with culture of coaching
- Managerial responsibilities for US-based individuals within a specific GRA project/portfolio, consisting of:
- Management of US based staff within Portfolio
- Resources overview and optimisation of work distribution within Product/Project teams in agreement with GRL/RA RDC Head/NARA Head - cross portfolio resources support as appropriate
- Organization of back-ups across group
- Provide advice on US-specific activities and ways of working, processes as mentor or coach; in this role, provide support, as needed, for meetings/teleconferences with US regulatory agency, if deemed appropriate in discussion with US-based individual in charge of the project and the respective GRL or RDC personnel.
- Escalate issues as appropriate
- Ensure the training of US-based personnel, and ensure completeness of training curriculum, in compliance with CIA
-Project-specific responsibilities:
° May be involved in review of US submissions, upon request of the Global Regulatory Lead (GRL) or NARA Head, to ensure adequacy/optimization of US-specific aspects within a submission.
- In their direct line to Head North America, the job holder will ensure:
° That regional strategic input is provided into RA project strategy and escalation as appropriate – i.e. ensure alignment and sharing of information/strategy across region and central GRA
° Attendance to NARA staff meeting
° Ensure alignment and adequate support of US Reg Ops
° Quality and process improvement within US
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