Regulatory Team Lead, Maintenance and CTA

(FCRS = US014) Novartis Pharmaceuticals Corporation; Barcelona; Ibrido; EUR 64.000 - 118.000; Tempo pieno

Descrizione del lavoro

Novartis Pharmaceuticals Corporation seeks a Regulatory Team Lead, Maintenance and CTA in Barcelona, hybrid role. You will lead a global regulatory team, ensuring timely clinical trial submissions and approvals while coaching staff and optimizing processes across functions.

The role requires strong regulatory expertise, strategic planning, and excellent communication in a cross-cultural environment. Base in Barcelona with hybrid work options and ongoing professional development opportunities.

Competenze

• Bachelor’s or Master’s degree in a science-related discipline with regulatory experience.
• Strong knowledge of global regulations, guidelines and regulatory processes.
• Proven ability to lead regulatory professionals and coach talent.
• Experience in strategic planning, regulatory review and submissions.
• Ability to drive process improvements and cross-functional collaboration.

Mansioni

• Lead and develop a global regulatory team delivering trial submissions and approvals.
• Coach team members to enable growth and capability building.
• Allocate resources effectively across portfolio balancing priorities and needs.
• Drive process improvement, simplification and automation for operational excellence.
• Build strong relationships with stakeholders and drive cross-functional collaboration.
• Champion Novartis culture, values and behaviours across teams.

Conoscenze

Regulatory leadership

People management

Regulatory strategy

Regulatory submissions

Formazione

Science degree

Descrizione del lavoro

Salary Range:

€63,600.00 - €118,000.00

Job Description Summary

#LI-Hybrid

Primary Location: Barcelona, Spain

Relocation Support: This role is based in Barcelona, Spain. Novartis is unable to offer relocation support: please only apply if accessible.

Shape how global clinical trials move forward. As Regulatory Team Lead, Maintenance and CTA, you’ll lead and develop a global regulatory team responsible for delivering high-quality, compliant and timely clinical trial submissions and approvals. You’ll combine people leadership with regulatory expertise, building strong partnerships across the organisation while driving smarter ways of working through simplification, continuous improvement and automation. It’s an opportunity to develop talent, influence how we work and help build a more agile, future-ready Regulatory Affairs organisation.

Job Description

Key Responsibilities

• Lead and develop a global regulatory team delivering high-quality, compliant and timely clinical trial submissions and approvals.
• Coach and support team members, building capability and enabling professional growth.
• Allocate resources effectively across the assigned portfolio, balancing priorities and business needs.
• Drive process improvement, simplification and automation to strengthen operational excellence.
• Build strong, customer-focused relationships with key stakeholders and act on feedback.
• Foster collaboration and knowledge sharing across Regulatory Affairs and global teams.
• Champion change and role-model Novartis culture, values and behaviours.

Essential Requirements

• Bachelor’s or Master’s degree in a science-related discipline, with relevant regulatory experience and demonstrated capability.
• Substantial knowledge and experience of global regulations, guidelines and processes supporting regulatory clinical trial activities.
• Demonstrated experience leading regulatory professionals, with strong people management, coaching and development capabilities.
• Strong experience in strategic planning, regulatory review, compliance, submissions and execution.
• Demonstrated ability to drive process improvement, simplification, automation and operational excellence.
• Strong communication, influencing and problem-solving skills within complex, cross-functional and international environments.

Benefits & Rewards

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.

Expected Annual Base Salary Range for role: €63,600 to €118,000

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.

In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Read our brochure to learn more about our global total rewards offering:

https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Commitment to Diversity and Inclusion / EEO paragraph

Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Skills Desired