The research conducted by our group is aimed at elucidating the causes and molecular mechanisms underlying neurodegeneration in Parkinson's disease (PD), a disabling and currently incurable neurodegenerative disorder. To this end, we conduct clinical and pre-clinical translational research in both patients with PD and human-relevant experimental in vitro and in vivo PD-related models. Data entry for Phase I, II, III and IV clinical trials and research projects in the field of neurodegenerative diseases.

Keep clinical data in Case Report Forms (CRFs) up to date using source documents. Attend site monitoring visits and review and resolve queries in accordance with Good Clinical Practice (GCP) guidelines. Contribute to the development of projects, in collaboration with medical and technical teams, aimed at improving the quality of life of patients with neurodegenerative diseases.

Education and qualifications: Required: Bachelor's degree in Biotechnology, Biology, Biochemistry, Pharmacy, Nursing or another relevant scientific discipline. Training in Good Clinical Practice (GCP) and clinical trial methodology is desirable. Excellent communication skills and a high level of fluency in written and spoken English. Good computer skills, including proficiency in Microsoft Office and email.

Experience with SAP management software (not mandatory). G. apps, wearable devices and remote monitoring). Knowledge of statistical packages such as SPSS, Stata and R, as well as experience with databases. Full-time (37,5 hours per week).

Contract type: Technical and scientific activities contract linked to project activities Incorporation into the 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 largest hospital in Barcelona and the largest within the Catalan Institute of Health (ICS). ~ A dynamic scientific environment of excellence, where cutting-edge biomedical projects are continuously developed. ~ Adaptable working hours. ~Flexible remuneration programme, including meal vouchers, health insurance, transport and more. ~ International mobility support (Welcome Services): we aim to make your arrival in Barcelona smooth and pleasant by providing city information, guidance on required procedures, access to the International Welcome Desk, family support and assistance with finding accommodation. Depending on the role, candidates may complete a case study, technical task, presentation, or written exercise, on-site or remotely. Education, references, and other job-related verifications may be carried out.

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.

Information on Personal Data Protection: Data Controller: Fundació Hospital Universitari Vall d'Hebron Institut de Recerca -VHIR-.

Legal Basis: Your consent.

Data retention period: If you are selected, as long as the employment relationship is in force and legal responsibilities may arise.

Data sharing: Rights: You can access, rectify, delete, object to, and limit the processing of data, as well as request data portability where applicable, by contacting [email protected].

Data Protection

Authority

📌 Study Coordinator de Ensayos Clínicos (Cataluña)
🏢 Vall D'Hebron Institute Of Research (Vhir) - Vall D'Hebron Institut De Recerca
📍 Cataluña