Senior Life Sciences Counsel - R&D Contracts

Ascendis Pharma

Denmark

On-site

DKK 900,000 - 1,300,000

Full time

9 days ago

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Job summary

Ascendis Pharma, a global biopharmaceutical company, seeks a Senior Legal Counsel (R&D) to support the full product lifecycle from discovery through commercial supply. You will draft, review and negotiate a broad range of contracts with laboratories, CMOs, CROs, hospitals and universities, ensuring compliant, value-driven solutions.

You will collaborate with our global R&D teams, advise on IP matters, and help advance our TransCon-based programs while integrating IT and digital health

Qualifications

  • At least 7–8 years as in-house counsel or law firm attorney in pharma or life sciences.
  • Experience drafting, reviewing and negotiating complex pharma contracts.
  • Experience supporting Product Supply and Quality and CMOs/CDMOs; advantage if with CMC.
  • Clinical trial agreements experience including site agreements and CRO contracts.
  • Solid understanding of IP rights in contractual contexts.

Responsibilities

  • Serve as legal partner to Product Supply and Quality on contracts and supply chain matters.
  • Negotiate and review trial site agreements, informed consent forms, and vendor contracts.
  • Draft, review, and negotiate confidentiality, service, research, license, collaboration, and material transfer agreements.
  • Provide legal support to Research, Medical Affairs, and Regulatory Affairs as needed.
  • Collaborate with stakeholders across Denmark, the US, and Germany to improve templates and processes.

Skills

Contract drafting
Contract negotiation
Clinical trial agreements
IP law
Product supply & quality
CRO/CMO contracts
Cross-functional collaboration

Education

Master's degree in Law

Job description

Ascendis Pharma, a global biopharmaceutical company, seeks a Senior Legal Counsel (R&D) to support the full product lifecycle from discovery through commercial supply. You will draft, review and negotiate a broad range of contracts with laboratories, CMOs, CROs, hospitals and universities, ensuring compliant, value-driven solutions.

You will collaborate with our global R&D teams, advise on IP matters, and help advance our TransCon-based programs while integrating IT and digital health

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