ppOrganisation/Company Fundació Privada Institut d'Investigació Oncològica de Vall d'Hebron (VHIO) Research Field Medical sciences » Cancer research Researcher Profile Other Profession Positions Master Positions Application Deadline 31 Dec 2026 - 00:00 (Africa/Abidjan) Country Spain Type of Contract Permanent Job Status Full-time Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No /p h3Offer Description /h3 pThe Vall d´Hebron Institute of Oncology (VHIO) Seeks a “bQuality Clinical Trials Technician /b” /p pbReference: /b /p pbNumber of vacancies: /b 1 /p pLocated within the Vall d´Hebron Barcelona Hospital Campus, our researchers closely collaborate and interact with Vall d´Hebron physician-scientists. Translational science and clinical research are therefore tightly connected which promotes superb interaction and teamwork which, in turn, accelerates the bench-bedside-bed cycle of knowledge. This privileged environment affords VHIO direct access to patients as well as the entire spectrum of oncology professionals who care for them, and a second-to-none appreciation of how cancer science can translate into more powerful, targeted treatments and better practice for the care of patients. /p pWithin VHIO,the Clinical trials quality team has the aim to improve quality and unify processes and standardize procedures in the clinical trials carried out. Quality is of paramount importance in performing clinical trials. Guaranteeing that all the current regulations of these studies are complied with is therefore essential. These homogeneous efforts follow Good Clinical Practice (GCP) guidelines, with the safety of patients as the top priority throughout. /p pbThe tasks to be carried out will be: /b /p ul liAssisting in the creation, review, revision and management of standard operation procedures in clinical trials.



/li liAssisting with the organization for regulatory inspections and audits – pre-planning, coordination, compilation of required documentation, the hosting and conducting of these activities, and follow-up. /li liCollect and compile quality statistical data. /li liPerform quality controls and participate in the review and the correct implementation of clinical trials related processes. /li liDocument internal audits and other quality assurance activities. /li liAnalyse data to identify areas for improvement in the quality system. /li liInterpretation and implementation of quality assurance standards. /li liProviding regulatory compliance guidance and quality improvement advice to the Medical Oncology Department. /li liReporting, managing and following deviations, complaints, issues, non-conformances and their related CAPAs. /li liMonitor risk management activities in clinical trials. /li liPrepare training materials and conduct trainings on relevant clinical trial quality assurance issues. /li liGuarantee ongoing compliance with quality and industry regulatory requirements. /li /ul pbRequirements: /b /p pbWhat do we need? /b /p ul liBachelor’s degree in life sciences (e.g. Pharmacy, Biology, Biotechnology). /li liFluency in both oral and written English. /li liKnowledge of QA tools, concepts, methodologies and relevant regulatory requirements. /li liExperience in Clinical Trials and Good Clinical Practice Quality Assurance. /li liExperience in quality inspection, auditing and testing as well as implementing corrective action programs. /li liExcel, Word, Power Point and database skills. /li /ul pComplementary: /p ul liBackground in Medical Oncology and hematology.



/li liBackground in Quality. /li /ul pbAdditional information: /b /p pbWe offer: /b /p ul liThe possibility of developing your professional career in a competitive environment. /li liTo be part of a center that is constantly developing, pursuing excellence in research and collaborating with leading teams. /li liWe offer and promote a diverse and inclusive environment, and welcome all people equally, regardless of age, disability, gender, nationality, race, religion or sexual orientation. /li liWe care about our environment and understand the importance ofsustainability.We have the GreenVhio program, which you can be a part of. /li /ul pbConditions: /b /p ul liPermanent contract. /li liSalary according to qualifications and experience following VHIO pay scales. /li liFlexible remuneration program (includes restaurant vouchers/cards, transport, medical insurance, and “baby daycare” voucher). /li liFlexible working hours and measures to balance work, family, and personal life, and promote gender equality, as established in the VHIO collective agreement. /li li24 days of holidays and 6 personal days. /li liFully subsidized Catalan, Spanish, or English courses. /li liTake advantage of doing sports at great prices with bUrban Sports Club /b. /li liYou’ll have access to weekly bphysiotherapy sessions /b at the office, offered at a reduced price for the team. /li /ul pbr/bVall d’Hebron Institute Oncology (VHIO) /bendorses the Requirements and Principles of the European Charter for Researchers, the Code of Conduct for the Recruitment of Researchers promoted by the European Commission and follows Equal Opportunities policies.br/ /p pOn 10th April 2018 VHIO was awarded the “HR Excellence in Research” logo. Our Institute was consequently granted permission to use the HR Excellence in Research Award logo as demonstration of its stimulating and favourable work environment in line with the Charter Code. /p /p #J-18808-Ljbffr

📌 2026-031-01 Quality Clinical Trials Technician (España)
🏢 Fundacio Privada Institut d'Investigacio Oncologica de Vall d'Hebron (VHIO)
📍 España