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Staff & Global R&D Legal Counsel

Lavoro temporaneo

Chiesi

Overview

In this role you will provide legal support across Staff functions and Global Research & Development to enable strategic projects while ensuring compliance with laws and internal policies. You will act as a business partner, guiding cross-functional initiatives and third‑party collaborations in line with Chiesi’s values and sustainability framework. The role involves drafting, negotiating, and managing R&D and vendor agreements, as well as advising on regulatory and quality matters affecting development activities. This position offers exposure to global projects at a leading biopharma group and opportunities to shape governance and risk management. You will work closely with diverse teams, 

Retribuzione / Benefits
  • pension
  • private medical insurance
  • wellbeing programme
  • flexible benefits programme
  • relocation support
  • remote work options
Responsabilità
  • Legal support to Staff Functions (Finance, Global Procurement, HR, Global Communications & Public Affairs)
  • Drafting, negotiating, and managing R&D and clinical/non-clinical study agreements
  • Legal advice on regulatory, quality, governance, and risk issues in R&D
  • Support for sustainability collaborations and multi-stakeholder initiatives
  • Legal support for Paolo Chiesi Foundation projects
  • Provide legal assessment and risk evaluation for cross-functional projects
  • Engagement with clinical sites, investigators, and research partners
  • Stand-alone research initiatives and industry collaborations with pharma/academia
  • Line manager oversight in all activities
Requisiti fondamentali
  • Master’s Degree in Law
  • 2–3 years of professional experience in a pharmaceutical company or leading international law firm
  • Fluency in English (written and spoken)
  • Strong problem-solving abilities and risk assessment
  • Good communication and teamwork skills
  • strong communication
  • teamwork
  • problem-solving
  • contract drafting and negotiation
  • R&D agreements management
  • regulatory and quality matters in clinical trials (GxP)
Offerta di lavoro pubblicata 2 giorni fa
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