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 spreading 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.
Clinical Research Quality Manager Quality, Process and Documentation Management Unit JOB DESCRIPTION Education and Qualifications:Required: Bachelor's Degree in Health Sciences.Additional training in Good Clinical Practice (GCP) - ICH E2 (R6).Fluency in Catalan, Spanish, and English (business level).Desired: Additional training in other Quality standards: ISO 9001 and Lean methodology.Knowledge of Validation of computerized systems. Experience and Knowledge:Required: At least 2 years of experience working in clinical research or quality departments.Personal skills: self-motivated, well organized, oriented to results, rigorous, flexible, and committed.Customer orientation, teamwork, and good problem-solving and communication skills are also required.Desired: Deep Knowledge of Clinical Trial operations.Experience in process analysis with Lean methodology. Main Responsibilities and Duties:Provide support to research teams before and during sponsor audits and inspections of health authorities.Promote compliance with Good Clinical Practice standards throughout the institution and research teams.Participate, develop, and implement the Clinical Research Quality Plan.Be an active member of the Clinical Trials Transversal Coordinating Group that carries out process analysis and continuous improvement for clinical research in Vall d'Hebron Campus.Analyze clinical research processes, anticipating and detecting improvement opportunities, as well as managing, registering, monitoring, and following up on quality findings and improvement opportunities.Write standard operating procedures related to Clinical Research when necessary, as well as other documentation.Participate in the validation of computerized systems when necessary.Conduct satisfaction surveys on IPs and Sponsors. Labour Conditions:Full-time position: 40 h/week.Starting date: Immediate.Gross annual salary: 28,000 - 35,000 euros (Remuneration will depend on experience and skills.
Salary ranges are consistent with our Collective Agreement pay scale).Contract: Open-ended contract linked to the project. What Can We Offer?Incorporation to Vall d'Hebron Research Institute (VHIR), a public sector institution that promotes and develops biomedical research, innovation, and teaching at Vall d'Hebron University Hospital (HUVH), the biggest hospital in Barcelona and the largest of the Catalan Institute of Health (ICS).
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