Global Head of Clinical Safety

Galderma; Cádiz; Presencial; EUR 70.000 - 90.000; Jornada completa

Descripción del empleo

Galderma is a leading dermatology company present in approximately 90 countries, offering a portfolio of premium brands in Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Founded in 1981, the company is dedicated to advancing dermatology to meet individual skin needs and improve outcomes in partnership with healthcare professionals.

We seek passionate, results-oriented individuals who value learning, positivity, teamwork, and collaboration. Our goal is to empower employees' growth while meeting business objectives, embracing diversity, and respecting personal rights.

We are establishing a new Global Capability Center in Barcelona, located in the Eixample District, providing opportunities for professional development and global project exposure.

Job Title: Global Head of Clinical Safety

Location: Barcelona, Spain (hybrid)

Job Description: The Global Head of Clinical Safety will oversee medical safety for products in clinical development, focusing on Nemolizumab. Responsibilities include signal detection, risk management, safety analyses, and managing PV relationships. The role involves medical review of safety data, team management across locations, and significant visibility within the organization, reporting to the Global Head of Pharmacovigilance Risk Management. Relocation support is available for suitable candidates.

Key Responsibilities:

1. Propose measures to minimize risks during clinical development and update Risk Management Plans.
2. Monitor safety profiles, validate signals, and recommend risk mitigation strategies.
3. Manage aggregate safety reports and develop Risk Management Plans.
4. Contribute to safety documentation for regulatory submissions and respond to safety questions.
5. Participate in safety-related meetings with investigators, KOLs, and IDMC, supporting due diligence.
6. Lead safety data reviews during trials and escalate issues to governance bodies.
7. Ensure compliance with PV audits and inspections.
8. Collaborate effectively with global regulatory, medical, clinical, and commercial teams.
9. Manage a team of up to 5 direct reports.

Skills & Qualifications:

• MD degree required.
• At least 12 years of global clinical safety/pharmacovigilance experience, with 3-5 years in team management.
• Deep knowledge of international clinical development and post-marketing regulations, especially for biologics.
• Experience liaising with health authorities in US, EU, and other regions.
• Understanding of global pharmacovigilance requirements for clinical and post-marketing phases.
• Additional degrees in pharmacology, pharmacovigilance, or epidemiology are preferred.

What We Offer:

• Inclusive environment reflecting diverse perspectives.
• Competitive compensation, bonuses, and benefits.
• Hybrid working model.
• Personalized career development.
• Ownership culture encouraging growth and accountability.

Next Steps:

• Initial virtual interview with recruiter.
• Follow-up interview with the hiring manager.
• Final panel interview with the team.

Our People: We value professionalism, collaboration, and diversity, creating a supportive environment where everyone can thrive.