Senior Pharmaceutical Lawyer
hace 3 semanas
Kymos Group is a leading European contract research organization dedicated to providing innovative services to the pharmaceutical industry. Our team is growing, and we are seeking a skilled Senior Pharmaceutical Lawyer to develop this role for all Group companies.
Job Summary: We are looking for a highly motivated and experienced Senior Pharmaceutical Lawyer to join our team. 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:
- Ensure adherence to all applicable laws, regulations, and internal policies as the Compliance Officer at Corporate level.
- 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.
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