As Global R&D Counsel based at our EU HQ in Amsterdam, you will provide primary legal support for R&D activities in Europe, as part of the Global R&D Legal team.
Counseling on clinical trial, privacy and data transfer.
Providing advice on transparency, regulatory compliance, informed consent, regulatory inspection, and pharmacovigilance issues.
Performing contract drafting and negotiation for clinical trial, confidentiality, research consultant, services, pre-clinical, bioequivalence, material transfer and collaborative research agreements.
Reviewing legal documents associated with clinical research.
Collaborating with the internal compliance team to ensure compliance with applicable laws and regulations as well as with internal policies
Law Degree with 2-3 year’s post qualification experience, ideally within a pharmaceutical company, law firm or academic setting.
Familiarity with European laws and regulations pertaining to research.
2-3 years’ of experience counseling research clients in Europe.
Team player with the ability to work cross functionally within a global team.
English language proficiency is essential, written & verbal.
Legal & IP
Pre - employment screening
Teva will carry out appropriate verification and legally permitted vetting prior to the confirmation of any offer of employment. More information on this verification and vetting will be provided if you reach this stage of the application process.
Associate General Counsel, Clinical & Labeling - Based in U.S
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