Legal Counsel

hace 2 semanas

Barcelona, España Kymos Group A tiempo completo

Kymos is a leading European contract research organization, with laboratories in Spain, Italy and Germany, and a Liaison Office in South Korea, dedicated to providing innovative services to the pharmaceutical industry.

**Position Overview**:
This role will also serve as the Compliance Officer of the Kymos Group and provide legal support across various departments, contributing to the company’s strategic objectives.

**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.

***

**Application Process**:

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