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 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, religion, age, disability, or race.
Clinical Research Monitor - Rheumatology 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 science
- Master's degree in science
Experience and Knowledge:
Required:
- More than 4 years of experience in clinical research and/or clinical trials data monitoring
- Excellent interpersonal and communication skills
- Highly organized
- Ability to work under deadlines
- Ability to work with human study participants
- Knowledge of auditing
- Knowledge of good clinical practice and regulatory requirements (i.e., personal data protection)
- Fluency in spoken and written English
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: 40h/week.
Starting date: immediate.
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