Legal Internship
3 settimane fa
Some of what you will do:
- Support the negotiation and revision of commercial agreements (e.g. contracts with Sponsors (Clients), suppliers, consultants, confidentiality agreements, etc.);
- Support the Business Units providing legal opinions/feedbacks, strategic or interpretative advice, offering solutions to problems in order to prevent or mitigate the risks concerning the structure and activities of the Company;
- Support the maintenance of the relationship with legal external consultant and oversee their work providing clear direction, guidance and support;
- Support the legal consultancy about Headquarters and subsidiaries issues;
- Support the proper conduction of all the activities related to the Company Governance, such as the preparation of all the documentation necessary for the Board of Directors meeting and Partners Meeting;
- Support the monitoring of the update of the specific legal regulation applicable to the global affiliates and support its implementation, promptly updating the CEO;
- Support the arrangement, revision of contracts in the Company templates to ensure compliance with applicable regulations, and the correspondence with the characteristics of a specific case;
- Prepare, review and draft other legal documents;
- Guarantee the constant updating of the Company compliance, compliance policies, procedures and support training throughout the Company functions, with specific training;
- Participate to internal/external meetings as the Company legal reference and negotiate the best interest of the Company, as needed;
- Archive all the legal documentation and prepare reports.
What you have:
- Master Degree in Law. Having completed forensic traineeship is a plus.
- Knowledge of commercial law, civil law and EU data protection law;
- Strong interest in working in the life science industry
- Fluency in English, written and spoken;
- Good knowledge and experience with Microsoft Office;
- Planning and organizational skills;
- Leadership and communication skills;
- Result-oriented;
- Team-working oriented.
What we offer:
We offer a competitive salary, bonuses, and other benefits together with the opportunity to develop your professional career with an expanding and growing international company.
Please read the information notice on the processing of personal data in the candidates’ information section of our company website.
Who we are:
OPIS is an International CRO with 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects.
OPIS extensive expertise covers all phases of drug-related trials, taking care of the Sponsor beyond the therapeutic area, offering also accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training.
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