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GSK
Mexico City, Mexico
(on-site)
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Full-Time
Job Function
Human Resources
Regulatory Project and Data Manager
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Regulatory Project and Data Manager
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Description
Site Name: Mexico City Torre MitikahPosted Date: Oct 21 2025
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. We're uniting science, technology, and talent to get ahead of disease together.
Are you passionate about driving impactful regulatory projects and managing data to support global health initiatives? In this role, you will collaborate with cross-functional teams to ensure regulatory deliverables are met efficiently and effectively. You will play a key role in planning, tracking, and managing regulatory data and projects, contributing to GSK's mission of getting ahead of disease together. This is an opportunity to grow your career, make a meaningful impact, and be part of a team that values innovation, collaboration, and inclusion.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Develop and Maintain Regulatory Plans: Independently build, manage, and update integrated Regulatory Development Plans (RDPs) to reflect the Global Regulatory Strategy, ensuring deliverables, timelines, and resource needs are accurately captured across all development phases.
- Manage Regulatory Work Packages: Add, remove, or adjust work packages within the RDP; maintain predecessor/successor logic; and ensure alignment with global strategy, accurately reflecting development stages and dependencies.
- Conduct Scenario Planning: Create and analyze alternative planning schedules to support decision-making at both the project and portfolio levels, and clearly communicate the impact of changes on regulatory timelines.
- Collaborate Cross-functionally: Partner proactively with functional plan owners (e.g., Medical, Safety, Clinical) and project managers to ensure alignment of regulatory plans within broader project plans and timelines.
- Support Governance Processes: Prepare regulatory inputs for key governance meetings, ensuring data is complete, accurate, and actionable for resource and portfolio decision-making.
- Forecast Resources and Costs: Build and maintain schedules to support forecasting of regulatory resources (FTE/IPE) and costs (EPE), in collaboration with regulatory project managers and stakeholders.
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Broad understanding of the pharmaceutical industry, drug development environment, and R&D processes and objectives.
- Project management experience, preferably in the pharmaceutical industry or in a regulatory environment.
- Ideally possessing knowledge of Regulatory Affairs responsibilities from pre-IND through post-approval
- Ability to work well both independently and within a matrix environment to ensure on-time delivery of objectives
- Advanced english
Preferred Qualifications
If you have the following characteristics, it would be a plus:
- Experience with project management principles and systems (e.g., Planisware), resource management and reporting features (e.g., Spotfire)
This is a hybrid role based in Mexico, offering flexibility to work both remotely and on-site. If you're ready to take the next step in your career and contribute to meaningful projects that make a difference, we encourage you to apply today!
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Your application is voluntary; therefore, you understand and consent that GSK, located at Real Mayorazgo 130, Torre M, Piso 20, Col. Xoco, Benito Juárez, Mexico City, will process your personal data to evaluate your candidacy in accordance with the candidate privacy notice, which can be consulted at Candidate Privacy Notice. Among the information you provide for this purpose, you may choose to give us personal data that will help ensure an inclusive selection process. Rest assured that your information will be treated with the utmost confidentiality, in compliance with applicable regulations, and will not be available to hiring managers or anyone outside the recruitment team. Help us maintain, together, an inclusive and welcoming environment. By submitting information, I confirm that I agree that it will be processed in accordance with the stated privacy notice.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Find more about life at GSK at www.gsk.com
Job ID: 80795098
Websitewww.gsk.com
US Headquarters: Philadelphia, PA
Size:10000+ employees
Founded: 1830
Type: Company - Public (GSK)
Industry: Biotech & Pharmaceuticals
Revenue: $10+ billion (USD) per year
Video: https://youtu.be/RBdgq5VTQmM
We are a science-led global healthcare company. We research and develop a broad range of innovative products in three primary areas of Pharmaceuticals, Vaccines and Consumer Healthcare.
We also have a significant global presence with commercial operations in more than 150 countries, a netwo...
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