Project Manager for the Start-Up Unit, Ref. 21-2026

Description

**THE PROJECT TO BE DEVELOPED:** Drive the launch of commercial clinical studies and trials, coordinating the necessary processes to ensure compliance with administrative, regulatory, and operational requirements. The selected candidate will act as the coordination point among sponsors, research teams, and various involved services, ensuring that studies commence within established timelines and meet required quality standards. **KEY RESPONSIBILITIES:** * Analyze the feasibility of commercial clinical trials in coordination with the research team and the sponsor. * Coordinate study start-up activities, ensuring adherence to established deadlines. * Define internal workflows for each trial and coordinate research teams and involved services. * Organize and participate in site selection visits with sponsors and the research team. * Prepare cost analyses for studies and negotiate financial summaries with sponsors. * Supervise contracts for commercial clinical trials and coordinate their initiation with Procurement and Billing teams. * Monitor activities carried out during the start-up phase and tasks delegated to the CTA. * Support the Strategic Projects Manager and the Quality Manager in unit initiatives. * Participate in billing follow-up meetings and in monitoring indicators with strategic partners. **WHAT WE OFFER:** * Indefinite-term contract. * Professional development aligned with the Institution’s growth. * Working week of 37.5 hours with flexible scheduling. * SJD T-Cuida Program, featuring initiatives and benefits aimed at promoting the physical, emotional, social, and professional wellbeing of our teams. * Possibility of hybrid work, according to the position’s needs. * Economic conditions between €35.000 and €40.000 gross per year, depending on experience and expertise provided. * Location in Esplugues de Llobregat. * Integration into an environment committed to equal opportunities, diversity, and inclusion. **THE PROFILE WE SEEK:** * University degree in Health Sciences. * Minimum 3 years’ experience managing or coordinating clinical trials. * Training in Good Clinical Practice (GCP). * Proficiency in Catalan and Spanish, and advanced English. * Familiarity with office software (Microsoft Office) and regulations applicable to clinical trials. **KEY COMPETENCIES:** * Organization and planning. * Coordination ability. * Negotiation and results orientation. * Interpersonal communication. * Teamwork. * Rigor and attention to detail. * Autonomy and initiative. * Analytical and problem-solving skills. * Adaptability and flexibility. Esplugues de Llobregat, 14/07/2026