Clinical Validation

**Job Reference**:

- 570_25_CS_WDC_RE2

**Position**:

- Clinical Validation & Pilot Studies Coordinator (RE2)

**Closing Date**:

- Tuesday, 23 September, 2025

**Reference**: 570_25_CS_WDC_RE2

**Job title**: Clinical Validation & Pilot Studies Coordinator (RE2)

**About BSC**
- The Barcelona Supercomputing Center - Centro Nacional de Supercomputación (BSC-CNS) is the leading supercomputing center in Spain. It houses MareNostrum, one of the most powerful supercomputers in Europe, was a founding and hosting member of the former European HPC infrastructure PRACE (Partnership for Advanced Computing in Europe), and is now hosting entity for EuroHPC JU, the Joint Undertaking that leads large-scale investments and HPC provision in Europe. The mission of BSC is to research, develop and manage information technologies in order to facilitate scientific progress. BSC combines HPC service provision and R&D into both computer and computational science (life, earth and engineering sciences) under one roof, and currently has over 1000 staff from 60 countries.

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We promote Equity, Diversity and Inclusion, fostering an environment where each and every one of us is appreciated for who we are, regardless of our differences.

**Context And Mission**
- The BSC’s Machine Learning for Biomedical Research Unit at the Life Sciences Department and Workflows and Distributed Computing Group at the Computer Sciences Department are looking for a Junior Research Engineer to support the definition of the stroke patient journey and, in particular, to estimate the associated costs for the Spanish healthcare system. This position is part of the AGAUR OneCareAI Producte project, a collaboration with the Sant Pau Research Institute, aimed at advancing stroke risk prediction to enhance prevention, enable continuous monitoring using AI, and explore commercial opportunities.
This role offers the opportunity to work in close collaboration with the Technology Transfer Office and national and international experts in stroke research.

**Key Duties**
- Coordinate ongoing and upcoming clinical pilot studies
- Act as liaison between clinical teams (neurologists, CROs, KOLs) and internal AI/tech teams
- Ensure compliance, supporting documentation, audits, and quality system implementation
- Manage study timelines, monitor progress, and proactively resolve operational and regulatory issues
- Support patient recruitment, data collection and integrity, site monitoring, and follow-up
- Lead preparation of ethics submissions and interface with regulatory authorities
- Contribute to clinical protocol development, interim analyses, and final reporting
- Provide input to the market access team on pharmacoeconomic impact based on clinical evidence

**Requirements**:

- Education
- PhD, Master’s, or equivalent degree in Life Sciences, Biomedicine, Pharmacy, or related discipline
- Essential Knowledge and Professional Experience
- 3+ years of experience coordinating clinical trials, preferably involving digital health or wearable technologies
- Hands-on knowledge of ICH-GCP and clinical study lifecycle (start-up to close-out)
- Strong project management skills, including planning, documentation, and stakeholder coordination
- Experience in managing multiple clinical studies simultaneously
- Proficiency in digital tools for project and data management (e.g., eCRF, CTMS, Power BI)
- Additional Knowledge and Professional Experience
- Familiarity with omics or AI-driven healthcare innovation
- Knowledge of regulatory approval processes (CE Mark, MDR, FDA)
- Experience with EU-funded research projects (e.g., H2020, AGAUR, ISCIII)
- Competences
- Fluent in Spanish and English, advanced Catalan
- Outstanding interpersonal and cross-functional communication skills
- Strong decision-making and problem-solving ability
- Autonomous and accountable, with a collaborative mindset
- Committed to quality and continuous improvement

**Conditions**
- The position will be located at BSC within the Computer Sciences Department
- We offer a full-time contract (37.5h/week), a good working environment, a highly stimulating environment with state-of-the-art infrastructure, flexible working hours, extensive training plan, restaurant tickets, private health insurance, support to the relocation procedures
- Duration: Open-ended contract due to technical and scientific activities linked to the project and budget duration
- Holidays: 23 paid vacation days plus 24th and 31st of December per our collective agreement
- Starting date: 16/10/2025

**Applications procedure and process**
- A full CV in English including contact details
- A cover/motivation letter with a statement of interest in English, clearly specifying for which specific area and topics the applicant wishes to be considered. Additionally, two references for further contacts must be included. Applications without this document will not be