Descripción de la oferta
Job Description
The Germans Trias i Pujol Research Institute (IGTP) is seeking to incorporate a superior technician with experience in molecular biology research projects, preferably in the field of neuromuscular diseases, to join the DM1-Hub project within the Neuromuscular Research Group of Badalona (GRENBA) at IGTP.
DM1-Hub aims to be the basis for the implementation of precision medicine aspects in Spain for the benefit of patients with Myotonic Dystrophy type 1 (DM1), prioritizing better diagnosis and optimisation in the use of soon-to-be-available treatments. The DM1-Hub project brings together a group of 80 professionals in research and clinical monitoring of DM1, including predoctoral, postdoctoral and senior researchers, as well as renowned research groups in the field of rare neuromuscular diseases and DM1. The multidisciplinary work team includes specialists in genomics, epigenetics, bioinformatics, biostatistics, proteomics, applied research and scientific dissemination, supported by an extensive network of around 70 health professionals (neurologists, neuropediatricians, neuropsychologists and nurses) across more than 40 hospitals in 8 Autonomous Communities who follow up with DM1 patients.
The project DM1-Hub is funded through a grant PMPER24/00007 from ISCIII for Research Projects on Rare Diseases, under the 2024 Call for Joint Missions of the Ministry of Health and the Ministry of Science, Innovation and Universities, within the PERTE for Vanguard Health and the Recovery, Transformation and Resilience Plan.
Main Responsibilities
Coordinate and oversee the reception, registration, and organization of biological samples from the hospitals participating in the DM1‑Hub project, ensuring compliance with project and quality requirements.
Manage the classification, processing, storage, and inventory control of biological samples and derivatives, ensuring their integrity and optimal conservation.
Independently perform and provide technical oversight of high‑molecular‑weight DNA extraction workflows, ensuring consistency and quality of results.
Design, implement, and monitor quality control procedures for genetic material destined for long‑read sequencing technologies.
Execute, optimise, and troubleshoot DNA extraction, quantification, and validation protocols, acting as a technical reference within the laboratory.
Evaluate and compare methodologies, develop protocol improvements, and analyse and interpret experimental results to support project objectives.
Prepare technical reports, laboratory documentation, and quality records, ensuring full traceability and compliance with applicable standards.
Oversee the maintenance, quality control, and continuous improvement of databases associated with sample management and laboratory workflows.
Contribute to drafting scientific documents, technical reports, project deliverables, and standard operating procedures.
Participate in and contribute to scientific meetings, training activities, collaborative discussions, and dissemination initiatives related to the project.
Qualifications And Experience
Master’s degree in a discipline related to the health sciences.
High level of spoken and written English.
Strong organisational, communication, and documentation skills.
At least 1 year of previous experience in molecular biology research projects.
Previous experience handling blood samples and in basic molecular biology techniques (nucleic acid extraction, PCR, etc.).
Previous experience in ELISA assays, cell culture, and/or long‑read sequencing technologies (e.g., Oxford Nanopore, PacBio) will be highly valued.
An organised, proactive, enthusiastic, self‑motivated person with strong teamwork skills.
What We Offer
Temporary contract linked to DM1‑Hub until December 2026 (funded through grant PMPER24/00007 from ISCIII).
Full‑time contract.
Starting date: August 1st 2026.
Gross annual salary range: 26,000–28,000 € (distributed over 12 payments).
Flexible payment: child‑minding vouchers and meal voucher.
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, offering a supportive, friendly and collaborative ecosystem to promote professional development.
Equal Opportunity
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.
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