.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 Unit VHIR 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 Description Education and Qualifications: Required: Bachelor's Degree in Law Desired: Master's Degree Experience and Knowledge: Required: At least 2-5 years of experience in a similar position Excellent organizational skills with a vocation of service and customer orientation Ability to work in teams Fluent in Catalan, Spanish, and English, both written and oral Desired: 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 amendments Provide legal advice in the field of clinical trials and EPAs Define institutional regulatory compliance processes related to clinical trials and EPAs Provide support in audit processes linked to clinical trials Labour Conditions: Full-time position: 40h/week Starting date: immediate Gross annual salary: Remuneration will depend on experience and skills