2026_153_RESEARCH COORDINATING NURSE IN CATALONIA FOR THE DM1-HUB PROJECT AND OTHER CLINICAL RESEARCH PROJECTS
JOB DESCRIPTION
MAIN RESPONSIBILITIES
- The contracted professional will be responsible for coordinating and monitoring participants enrolled in the DM1-Hub project, including contacting adult and pediatric patients and organizing study visits across multiple participating hospitals in Barcelona. Key responsibilities will include collecting clinical information through telephone and in-person visits, administering clinical scales and assessments, assisting participants in completing patient-reported outcome measures (PROMs), entering and validating data in the REDCap database, and identifying and resolving missing data. The individual will also participate in regular meetings with DM1-Hub investigators and team members, manage the processing, labeling, storage, and shipment of biological samples to the IGTP-GRENBA laboratory, contribute occasionally to patient workshops and scientific events, and regularly report project
- Coordinate the DM1-Hub study visit staff, including the organization of training activities, ongoing supervision, and performance follow-up.
- Ensure the maintenance of study records, monitor data quality, and implement quality control procedures to guarantee the accuracy, completeness, and consistency of collected data.
- Contribute to the continuous improvement and updating of study protocols, including the identification and implementation of new clinical and research variables relevant to project objectives.
- Support the coordination of clinical trials conducted by the Neuromuscular Research Group at Hospital Universitari Germans Trias i Pujol, working closely with principal investigators, study coordinators, sponsors, monitors, and clinical staff.
- Coordinate participant recruitment activities, study visits, and follow-up schedules in accordance with study protocols and timelines.
- Verify compliance with study protocols, and resolve data queries, and conduct regular data quality reviews and monitoring procedures.
- Prepare study documentation for monitoring visits, audits, and inspections, ensuring that regulatory and study records are maintained appropriately.
- Coordinate the collection, processing, storage, and shipment of biological samples according to protocol-specific requirements.
- Act as a liaison between investigators, study participants, sponsors, contract research organizations (CROs), monitors, and healthcare professionals involved in clinical research activities.
- Support investigators in participant recruitment, retention, and follow-up processes.
- Participate in scientific research activities, including literature reviews, data analysis, interpretation of results, and preparation of scientific reports.
- Contribute to the preparation of abstracts, posters, oral communications, grant applications, and scientific manuscripts for publication in peer-reviewed journals.
- Present study findings at national and international scientific meetings and congresses and actively contribute to the dissemination of research results.
- Collaborate with multidisciplinary teams and external partners in the development of observational studies, patient registries, and clinical research projects related to neuromuscular diseases, including myotonic dystrophy type 1 (DM1).
- Participate in research strategy discussions and contribute to the identification of new research opportunities, study initiatives, and collaborative projects within the neuromuscular field
QUALIFICATIONS AND EXPERIENCE
- Nurse degree
- Skills in blood extraction
- Used to work with patients (adults and children)
- 2 years of previous experience in hospital work
- Microsoft office skills
- Languages spoken and written: Spanish and Catalan (English would be valued)
- Skills in coordinating patients’ agendas
- Skills in communication
- Open to work in more than 10 hospitals of Barcelona
- Open to make visits at home
- Interest in research and willing to learn new skills
- Skills and Professional Experience in coordinating work teams
- Skills and Professional Experience in coorfinating multiple projects
WHAT WE OFFER
- Type of contract and working hours: Permanent, full-time employment contract (under the Spanish Science Law / Ley de la Ciencia).
- Expected starting date: 1th of January 2027.
- 36.000 €/year.
- Gross annual remuneration inherent to the square objected to this call, will be fixed based on the experience provided and the skills of the candidate, distributed in 12 payments.
- Flexible payment (childminding vouchers).
- Coverage of transportation expenses for travel to the centres where patient visits are conducted or for biological sample collection
- 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.
