Regulatory Affairs Associate

buscojobs España; Barcelona; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading company in Barcelona seeks a Regulatory Affairs Strategist to deliver innovative global regulatory strategies for clinical trial registrations. This role focuses on regulatory submissions, health authority interactions, and leading compliance efforts to support the global business objectives. Ideal candidates will possess significant experience in regulatory affairs and demonstrate excellent communication and teamwork skills.

Servicios

Competitive compensation package

Bonus structure

Extended benefit package

Flexible hybrid work culture

Personalized career path development

Diversity and inclusion initiatives

Formación

• Experience interfacing with regulatory agencies.
• Ability to communicate regulatory strategies effectively.
• Demonstrated ability to work in cross-functional teams.

Responsabilidades

• Creating and managing clinical trial regulatory strategy.
• Oversight of regulatory submissions and ensuring compliance.
• Managing health authority interactions.

Conocimientos

Knowledge of regulatory requirements

Experience with regulatory submissions

Communication skills

Team interaction skills

Ability to identify issues

Adaptability to change

Descripción del empleo

The Regulatory Affairs Strategist delivers innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities. The RA Strategist is responsible for regulatory aspects related to clinical trial regulatory submissions in alignment with the global business strategy and in partnership with the functional subject matter experts within the Global R&D.

Key Responsibilities

• Creating and managing clinical trial regulatory strategy for biologics, executing clinical trial regulatory activities in alignment with agreed clinical timelines, including responses to health authority queries, amendments to clinical trial dossiers, regulatory SUSAR reporting, or any other regulatory activities as needed.
• Oversight of clinical trial regulatory submissions, ensuring accurate and compliant dossiers.
• Archiving clinical trial documentation.
• Managing health authority interaction for assigned regions in alignment with agreed regulatory strategy.
• Identifying and assessing risks associated with the clinical regulatory submissions and recommend strategies to mitigate these risks.
• Providing regular updates to global regulatory lead and indication regulatory leads regarding specific clinical trials.
• Managing of outside vendors.

Skills & Qualifications

• Knowledge and understanding of regulatory requirements for pharmaceutical / biological product development.
• Experience with performing regulatory submissions in at least one key regulatory region.
• Experience with communicating the regulatory strategy, issues, and risks in written and verbal format to regulatory senior leadership team and other governing bodies.
• Experience interfacing with regulatory agencies and skill at implementing successful regulatory strategies.
• Experience with documenting regulatory strategies in coordination with clinical plans and marketing objectives.
• Excellent team interaction skills along with demonstrated ability to work on a cross-functional team.
• Ability to identify opportunities / major issues and to communicate impact
• Demonstrated ability to deal with rapid change

What we offer in return

• You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.
• You will receive a competitive compensation package with bonus structure and extended benefit package.
• You will be able to work in a hybrid work culture.
• You will participate in feedback loops, during which a personalized career path will be established.
• You will be joining a growing company that believes in ownership from day one where everyone is empowered to grow and to take on accountability.

Next Steps

• If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
• The next step is a virtual conversation with the hiring manager.
• The final step is a panel conversation with the extended team.

Our people make a difference

At Galderma, you’ll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.