.Vall d'Hebron Research Institute (VHIR) is a public sector institution that promotes and develops the research, innovation, and biosanitary teaching of the Vall d'Hebron University Hospital.
Through the excellence of our research, we identify problems of society and contribute to spread them around the world.
In April 2015, the Vall d'Hebron Research Institute (VHIR) obtained the recognition of the European Commission HR Excellence.
This recognition proves that VHIR endorses the general principles of the European Charter for Researchers and a Code of Conduct for the Recruitment of Researchers (Charter & Code).
VHIR embraces Equality and Diversity.As reflected in our values, we work toward ensuring inclusion and equal opportunity in recruitment, hiring, training, and management for all staff within the organization, regardless of gender, civil status, family status, sexual orientation, religion, age, disability, or race.Lawyer for Clinical Trials/Clinical Projects/IPR Legal UnitVHIR offers a vacant position for a lawyer with experience in various areas of the Healthcare environment to develop tasks within the Legal Unit.
This unit ensures regulatory compliance in all institutional acts, especially in biomedical research projects and intellectual property (IP).
The unit aims to give advice to the scientific community at VHIR regarding continuous legal developments that affect biomedical research and the transfer of results to society.Job DescriptionEducation and Qualifications:Required: Bachelor's Degree in LawDesired: Master's DegreeExperience and Knowledge:Required:At least 2-5 years of experience in a similar positionExcellent organizational skills with a vocation of service and customer orientationAbility to work in teamsFluent in Catalan, Spanish, and English, both written and oralDesired: Specific knowledge in pharmaceutical and healthcare law and/or previous experience in the field of biomedical research (specifically in the field of clinical trials and EPAs)Main Responsibilities and Duties:Participate in the process of drafting, negotiating, and reviewing clinical trial contracts and amendmentsProvide legal advice in the field of clinical trials and EPAsDefine institutional regulatory compliance processes related to clinical trials and EPAsProvide support in audit processes linked to clinical trialsLabour Conditions:Full-time position: 40h/weekStarting date: immediateGross annual salary: Remuneration will depend on experience and skills