Director, Safety Physician

Singular: Building Brilliant Biotechs; Turbigo; In loco; EUR 120.000 - 180.000; Tempo pieno

Descrizione del lavoro

Singular: Building Brilliant Biotechs is seeking a Safety Physician at the Director level to own the global safety strategy for multiple development programmes. This role demands a medically trained safety leader with 10+ years of experience, focusing on shaping safety strategies in rare diseases and neurology. You will influence design and assessment, conduct benefit-risk assessments, and represent safety on cross-functional teams. The position requires a deep understanding of global PV regulations and the ability to lead high-impact safety discussions.

Competenze

• 10+ years of experience in the biopharmaceutical industry.
• Track record of owning safety strategy for development programmes.
• Experience in rare disease or neurology.

Mansioni

• Own the global safety strategy for multiple development programmes.
• Lead signal detection and benefit-risk assessments.
• Shape safety thinking early in development.

Conoscenze

Safety strategy development

Risk-benefit assessment

Signal detection

Cross-functional team collaboration

Global PV regulations knowledge

Formazione

MD or MD/PhD

Descrizione del lavoro

Safety Physician – Director Level

Global Development | Rare Disease & Neurology | UK

You are a medically trained safety leader who wants to move beyond execution and play a defining role in how development programmes are designed, challenged and advanced.

We are partnering with a European headquartered, science‑driven biopharmaceutical company with a growing global development portfolio. As the organisation expands its pipeline, it is bringing more strategic safety leadership in‑house to support complex, non‑oncology programmes in rare disease and neurology.

This is a Director‑level role with full ownership of multiple assets across development. You will not be a purely operational pharmacovigilance lead; instead, you will act as the safety thought‑partner to clinical, regulatory, biostatistics and governance teams, shaping risk–benefit strategy from early development through Phase III.

What You Will Do

You will own the global safety strategy for multiple development programmes, giving you real authority to influence how assets are designed, assessed and advanced. Rather than reacting late, you will shape safety thinking early, improving study quality, reducing regulatory friction and supporting faster decision‑making.

You will provide strategic input into protocols, IBs, ICFs, SAPs and DSURs, ensuring safety approaches are scientifically sound, proportionate and patient‑centred. Your judgement will directly influence how risk is communicated and managed across programmes.

You will lead signal detection, benefit–risk assessments and safety governance discussions, acting as a trusted medical voice in high‑impact decisions. By anticipating regulatory expectations, you will help submissions progress with fewer questions and delays.

Working at the centre of development, you will represent Safety on cross‑functional teams, partnering closely with clinical and regulatory colleagues to align safety strategy with programme and corporate goals.

About You

You are a medically trained safety physician (MD or MD/PhD) with around 10+ years of industry experience, and a track record of owning safety strategy for development programmes.

You bring experience in rare disease, neurology or other complex non‑oncology indications, along with a strong working knowledge of global PV regulations (EMA, FDA, ICH, CIOMS).

Practicalities

• Director‑level, permanent role
• UK‑based
• Ownership of multiple programmes across development stages

If you are a strategic safety physician who wants real influence over how programmes are built, apply now.