Scientific Clinical Monitor_Rheumalogy Research Group_20240313

.VHIR-RRHH-FOR-003_vs02The 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 and apply new solutions to the health problems of society and we 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, gender identity and expression, religion, age, functional diversity or ethnicity.Position: Scientific Clinical MonitorRheumatology Research GroupVHIR offers a Scientific Clinical Monitor position looking for a self-motivated person with experience in clinical research and/or clinical trial data monitoring.Job DescriptionEducation and Qualifications:Required:Bachelor's degree in scienceMaster's degree in scienceDesired: Fluency in Spanish and EnglishExperience and Knowledge:Required:More than 4 years of experience in clinical research and/or clinical trials data monitoringExcellent interpersonal and communication skillsHighly organizedAbility to work under deadlinesAbility to work with human study participantsProficient in word processing and database applicationsKnowledge of auditingKnowledge of good clinical practice and regulatory requirements (i.E. personal data protection)Main Responsibilities and Duties:Supporting CRFs and variables dictionaries developmentCoordinating and executing all aspects of the clinical monitoring process in accordance with good clinical practice and regulatory requirements (such as data entry, queries resolution, and data curation)Training and supporting clinical research personnel at collaborating sites in protocol procedures and implementationReviewing data collection for accuracy and completenessMonitoring reports of the project statusIdentifying problems in protocol implementationReviewing/solving regulatory issuesInterfacing with clinical investigators, medical staff, management, lab technicians, and informaticiansReporting ongoing work and site-level problems to the Scientific Project Manager and project coordinatorsTraveling to collaborating sites (if needed)Labour Conditions:Full-Time position (40 hours per week)Salary: 24.000-26