Clinical Research Attorney
1 mese fa
At AbbVie, we seek a seasoned attorney to collaborate with our global R&D organization, providing strategic legal and business guidance.
The ideal candidate will be responsible for identifying and resolving complex legal issues, drafting and negotiating agreements, and working with internal stakeholders and third-party partners.
- Drafting, reviewing, and negotiating clinical study and collaborative research agreements, services agreements, and other R&D agreements.
- Developing and reviewing patient informed consent forms and incorporating feedback from regulatory authorities and/or ethics committees.
- Serving as a subject matter expert on R&D legal and regulatory matters in the EU with a focus on Italy.
- Conducting training on R&D legal and regulatory issues.
- Advising the AbbVie Clinical Development and Medical Affairs organizations on clinical research activities.
- Communicating legal guidance on complex matters related to clinical research, including study participant privacy and rights, data integrity, and digital health.
The successful candidate will possess a law degree and meet the professional licensing requirement applicable in the European Union, with at least five years of experience advising on R&D clinical legal issues in the EU region with a focus on Italy.
Requirements:
- Law degree and professional licensing in the European Union.
- At least five years of experience advising on R&D clinical legal issues in the EU region with a focus on Italy.
- Excellent legal analysis skills, good judgment, and ability to identify and quickly address critical issues.
- Strong interpersonal skills, including diplomacy and flexibility.
- Ability to work well independently and on a team, and prioritize multiple matters.
- Proficiency in Italian and English.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving its community, and embracing diversity and inclusion.
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