2026_155_CLINICAL DATA MANAGER - GRENBA
JOB DESCRIPTION
to incorporate a Clinical Data Manager to work on the INTEGRA-DM1 and DM1 Hub
project database, the largest clinical registry of patients with Myotonic Dystrophy Type
1 (DM1) in Spain.
INTEGRA-DM1 is a complex multiomics project and DM1-Hub is a national clinical
registry and research platform that supports clinical research, translational studies, and
real world evidence generation in DM1. Due to the growing volume and complexity of
the data, we currently need a professional with a transversal vision and strong analytical
capacity to process and analyse clinical data in order to support strategic decision
making, while responding to the evolving needs of the research group. The selected
candidate will lead the development of a digital application to enable the prospective
follow-up of patients, contributing to the construction of a natural history registry of the
disease through the systematic collection of a wide range of Patient Reported Outcome
Measures (PROMs). In addition, the selected candidate will give support to the ongoing
long-read genomic data analyses and lead exploratory studies combining omics and
clinical data in order to better characterize the generated DM1-INTEGRA data and the
existing DM1 cohort of the registry.
MAIN RESPONSIBILITIES
and the DM1-Hub project database. Developing of graphical user interfaces
(GUIs).
b) Building and maintaining pipelines, coding in Nextflow, R, Python, and Bash.
c) Apply a transversal and integrative analytical approach to support strategic
decision making related to the evolution and sustainability.
d) Respond to data-related needs of the research group, translating clinical and
scientific questions into analytical solutions.
e) Ensure data quality, harmonisation, standardisation, and interoperability of
clinical datasets.
f) Design and lead the development of a digital application for prospective patient
follow-up, enabling systematic data capture over time.
g) Implement and analyse a wide range of Patient Reported Outcome Measures
(PROMs) to support the study of the natural history of DM1.
h) Generate reports, visualisations, and scientific outputs for internal decision
making, publications, and project deliverables.
i) Ensure compliance with ethical, regulatory, and data protection requirements
related to clinical research data.
QUALIFICATIONS AND EXPERIENCE
related disciplines.
b) Strong background in (bio)informatics and large-scale clinical and omics data analysis,
especially genomics (long-read) and proteomics.
c) Demonstrated experience in processing, integrating, and analysing complex clinical or
biomedical datasets.
d) Experience in designing and developing web and/or mobile applications (TRL 1-5),
preferably in a clinical or healthcare research environment.
e) Proficiency in data analysis, workflow architecture tools (Nextflow, Snakemake) and
programming tools (e.g. R, Python, SQL or similar).
f) Excellent written and spoken English and Spanish; knowledge of Catalan will be
valued.
g) Strategic mindset, strong problem-solving skills, autonomy, and ability to collaborate
in multidisciplinary teams.
WHAT WE OFFER
- Type of contract and working hours: Permanent, full-time employment contract (under the Spanish Science Law / Ley de la Ciencia).
- 1 of January 2027.
- 38.000 €/year.
- Flexible payment (childminding vouchers).
- 23 days holiday and 5 days for personal matters.
- Training capsules by the company.
- Be part of an excellent multidisciplinary research centre with the HRS4R badge.
- Location on the Can Ruti Campus, a first-class translational research environment in the Barcelona area, in a very stimulating scientific environment.
- The IGTP offers a supportive, friendly and collaborative ecosystem to promote professional development and help you achieve your research goals.
FOR MORE INFORMATION
HOW TO APPLY
- Motivation letter explaining their interest in the position.
- Updated CV.
- Contact of 2-3 references.
- Curricular evaluation: analysis of the curriculum vitae to assess aspects related to training, professional career and experience in positions related to the job position under selection.
- Personal interview: once the résumé has been evaluated, the selected candidates will be called for a personal interview to verify and expand on the information detailed in the résumé and to evaluate aspects related to experience and professional skills.
DEADLINE FOR APPLICATIONS
About us
The Germans Trias i Pujol Research Institute (IGTP) is a public research centre located in Badalona. Its main objective is to increase scientific knowledge in order to transform it into solutions to improve the health and medical care of patients and the community.
The Institute is associated with one of the major university hospitals in the Barcelona area, the Germans Trias i Pujol Hospital, and is part of the Can Ruti biomedical campus. IGTP is a CERCA centre and is also accredited as a centre of excellence by the Instituto de Salud Carlos III (ISCIII) and is in charge of coordinating the management and scientific strategy of the campus, working in close collaboration with the other centres.
The Germans Trias i Pujol Research Institute carries out research within 9 areas:
- Cancer
- Cardiovascular and Respiratory Diseases
- Community Health
- Diseases of the Liver and Digestive Tract
- Endocrine and Diseases of the Metabolism, Bones and Kidneys
- Immunology and Inflammation
- Infectious Diseases
- Neuroscience
- Science of Behaviour and Substance Abuse
The following video is a bird's eye view of Campus Can Ruti a top-tier translational research environment in the Barcelona area, in a very stimulating scientific environment. The IGTP offers a supportive, friendly and collaborative ecosystem to promote professional development and help you achieve your research goals.
The IGTP, in its commitment to equal opportunities, guarantees equal treatment between candidates and persons with a degree of disability equal to or greater than 33 per 100, as accredited by the Spanish Autonomous Regions or the State Administration, or who have been declared to have a total permanent disability in a different profession through a resolution of the National Institute of Social Security, while retaining functional capacity for the completion of the tasks of the post will be positively considered.
