As Regulatory Operations Manager, you will be responsible for leading or supporting strategic and operational Regulatory projects, which support business strategy and platform delivery.
This role will provide YOU the opportunity to lead key activities to progress YOUR career.
These responsibilities include some of the following
- Fulfil standard, ad hoc, or complex data reporting request and design outputs.
- Assist Regulatory Business Operations (RBO) staff in delivery of projects.
- Assist RBO staff in process documentation, monitoring, and reporting.
- Maintain Team sites.
- Adhere to records retention.
- Complete appropriate training.
- Assist Regulatory Business Operations staff to optimize project plan robustness (scope, deliverables, resources, timing).
- Provide project support to meet assigned business deliverables.
- Edit existing process documentation and lead monitoring and reporting.
- Provide analysis and interpretation of information in response to requests from requestors and pursue greater data quality through identification of gaps and delivery of efficient solutions.
Basic Qualifications:
- bachelors degree.
- 3 years of pharmaceutical industry experience in a regulatory environment.
- Experience with License Maintenance as we'll as overall RD processes.
- Direct experience with project planning execution.
Preferred Qualifications:
- masters degree or MBA
- Experience working in a matrixed environment
- Demonstrated ability to engage and influence senior stakeholders.
Why GSK
- Operating at pace and agile decision-making using evidence and applying judgement to balance pace, rigour and risk.
- Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
- Continuously looking for opportunities to learn, build skills and share learning.
- Sustaining energy and we'll-being.
- Building strong relationships and collaboration, honest and open conversations.
- Budgeting and cost-consciousness.