Senior Legal Counsel - Inklusiver Job

Boehringer Ingelheim; Ingelheim am Rhein; Hybrid; EUR 80.000 - 100.000; Vollzeit

Zusammenfassung

A leading pharmaceutical company in Ingelheim is seeking a legal professional to join their Human Pharma team. This fixed-term position, lasting for one year, offers a hybrid work model and the opportunity to contribute to innovative medicine initiatives. Ideal candidates will have a bar qualification from a European country, strong expertise in pharmaceutical law, and excellent communication skills in English. Responsibilities include acting as a legal partner and advising various teams on regulatory and quality matters.

Qualifikationen

• Legal professional with bar qualification and long-term experience, ideally in pharmaceuticals.
• Strong expertise in regulatory, quality, and pharmacovigilance matters.
• Solid understanding of GCP framework in clinical trials.

Aufgaben

• Act as a trusted legal business partner for Corporate Medicine.
• Deliver legal assessments for innovative business initiatives.
• Monitor legal developments and their business impact.
• Enhance contract templates for real-world evidence generation.
• Collaborate cross-functionally to foster a solution-oriented culture.

Kenntnisse

Pharmaceutical law expertise

Regulatory affairs knowledge

Stakeholder management skills

Communication in English

Ausbildung

Bar qualification in a European country

Jobbeschreibung

The Position

Be part of a purpose-driven Legal Human Pharma team in Ingelheim, where your legal expertise directly enables innovation in medicine and patient‑centric initiatives. Work at the intersection of laws and science and advise on cutting‑edge initiatives that bring impact to generations.

This is a fixed‑term opportunity for 1 year (planned to start mid‑January 2026) to cover parental leave, offering a hybrid working model and the chance to make a meaningful impact from day one.

Tasks & responsibilities

• Act as a trusted legal business partner for the Corporate Medicine function, advise Regulatory Affairs, Quality Medicine, Patient Safety teams and real‑world evidence topics.
• Deliver legal assessments and co‑develop solutions that enable the innovative business initiatives.
• Monitor and interpret legal developments, evaluate their impact on business operations and strategic initiatives.
• Streamline processes and contribute to the enhancement of contract templates for the real‑world evidence generation.
• Collaborate cross‑functionally and globally to foster a proactive and solution‑oriented culture.

Requirements

• Legal professional with bar qualification in one of the European countries or equivalent, long‑term legal practice experience, ideally in the pharmaceutical industry.
• Strong expertise in pharmaceutical law, regulatory, quality, and pharmacovigilance matters for medicine development and commercialization.
• Solid understanding of the GCP framework and its legal implications in clinical trials.
• Experience with real‑world evidence generation is a plus.
• Excellent communication in English and stakeholder management skills.

Ready to contact us?

If you have any questions about the job posting or process - please contact our HR Direct Team, Tel: [phone]‑3330 or via mail: hr.de@boehringer‑ingelheim.com.

Recruitment process

1. Online application – the job posting is online until December 12th, 2025.
2. Virtual meeting in the week of 15th December.
3. On‑site interviews beginning / mid‑January.