Senior Legal Counsel

hace 1 mes

Barcelona, Barcelona, España Kymos Group A tiempo completo

Job Title: Legal Counsel – Pharmaceutical

Job Summary:

Kymos Group, a leading European contract research organization, seeks a skilled Legal Counsel to develop this role for all Group companies. The ideal candidate will have 3-4 years of experience in the pharmaceutical or biotech industries and a deep understanding of regulatory compliance, intellectual property, and contract law.

Key Responsibilities:

  • Serve as the Compliance Officer at Corporate level, ensuring adherence to all applicable laws, regulations, and internal policies.
  • Coordinate the legal practices between headquarters and affiliates, collaborating with external legal services of each legal entity, when necessary.
  • Draft, review, and negotiate business contracts, including NDAs, MSAs, QTAs, clinical trial agreements, and partnership agreements.
  • Draft, review, and negotiate general supply agreements, purchase contracts, and vendor agreements.
  • Ensure compliance with data protection laws and regulations, including GDPR, and advise on data privacy matters.
  • Coordinate with the Board Secretary on corporate governance matters, including the preparation of corporate documents, minutes, resolutions, powers of attorney, and other related matters.
  • Oversee the management of insurance policies, ensuring adequate coverage for various legal and operational risks.
  • Collaborate with Human Resources in managing the relationship with the works council, addressing labor relations issues and ensuring compliance with employment laws.
  • Represent the company in legal disputes and coordinate with external counsel as needed.
  • Stay updated on legal developments and trends within the pharmaceutical sector; advise on legal matters related to drug development, regulatory compliance, and marketing practices.

Qualifications:

  • Licensed to practice law.
  • 3-5 years of experience in a legal role within the pharmaceutical or biotech industry.
  • Substantial understanding of EMA, FDA regulations, legal compliance, and contract law.
  • Proven experience drafting and negotiating NDAs, MSAs, and QTAs.
  • Familiarity with risk management and risk assessment.
  • Ability to work independently and as part of a team.
  • Strong analytical and problem-solving skills.
  • Effective communication skills, both written and verbal.
  • Excellent drafting and negotiation skills in English.

What We Offer:

  • Competitive salary (including yearly bonus) and benefits package (partial teleworking, flexible labor time, flexible retribution).
  • Opportunities for professional development and advancement.
  • International position working in a multicultural environment.
  • A collaborative and inclusive work climate.
  • The chance to make a meaningful impact on medicines market access.

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