Compromiso con "HR Excellence in Research" We are looking for a self-driven and committed Project Manager to join the Project Management Office (PMO) at Foundation Sant Joan de Déu to provide daily scientific, technical and managerial support to European projects of the Project Management Office portfolio.
The International Post-Award Unit runs a portfolio of more than 50 European projects (mainly from European Commission- Horizon 2020 and Horizon Europe), 10 of which are coordinated by our institution. The International Post-Award Unit includes a Project Management Office (PMO) offering support to Principal Investigators from IRSJD and other researchers from Sant Joan de Déu ecosystem in project coordination. Our project manager's team provides daily scientific, technical and managerial support to Principal Investigators to help them successfully develop their international projects.
The candidate will be integrated into the PMO and shall be responsible for the effective implementation of the assigned projects ranging from Health to Social fields. The person we are looking for must be proactive, responsible, creative, flexible, empathic, and service-oriented. He/she should be comfortable working on long-term strategic plans as well as day-to-day project management tasks.
Key responsibilities General coordination of European projects.Interface between the project coordinator and internal team/partners or external stakeholders, translating coordinator's decision-making into actions.Coordination of day-to-day internal scientific/technical work according to the work plan.Coordination of Work package where SJD is the leader, organization of meetings, collect state of the art of clinical practice, and elaborate required documents.Writing guidelines, activity reports, and deliverables where SJD is responsible.Preparation of agendas and presentations for project meetings and related committees (advisory board, external experts), participation in meetings, drafting minutes, and chairing meetings.Providing guidance to project partners (scientific orientation, mitigation plan, ethical issues, work plan).Resolution of conflicts, orientation of partners toward work plans, guidance of the consortium toward objectives.Project quality and risk management (revision of all final documents as deliverables, communication, patient-related material, exploitation plan).Elaboration of a Data Management Plan and DPIA. Data management plan follow-up. Monitoring of data protection compliance.Monitoring of ethical regulatory processes and compliance.Gantt chart follow-up, management of timelines and deadlines.Daily management activities, organization of meetings and events linked to the project, administrative tasks.EC Portal monitoring (uploading deliverables, milestones, outputs).Economic follow-up, looking for providers and quotes, support in drafting amendments.Minimum Requirements PhD (ideally in health or related psycho-social field).Scientific background and understanding of both qualitative and quantitative research approaches, including methods, techniques, and the underlying theories.Ability to write technical and scientific content, guidelines, reports.1-3 years of experience in a position of Scientific Manager or coordination of a research European project.Good knowledge of main rules and regulations affecting European Projects, familiarity with EU funded projects and project management.Strong organization and time management skills. Ability to prioritize and organize project workload and meet time-critical schedules.Leadership, ability to lead and give orientation.Ability to work under pressure with strict deadlines while maintaining accuracy and thorough attention to detail.Good communication skills, especially the ability to negotiate and reach consensus.English proficiency. Spanish advanced level.Good interpersonal skills and the ability and flexibility to liaise with a variety of people.Proactivity, and oriented to problem-solving.Ability to work independently as well as part of a team.Good numeracy skills with the ability to present and interpret financial reports.Additional skills of interest: Knowledge of transversal issues valued such as ethical/regulatory processes, clinical trials, data management, intellectual property, dissemination.We offer: Full-time contract with a trial period of 4 months.Estimated starting date: September 2024.Economic conditions according to profile and knowledge provided.Possibility for remote work up to two days per week.Continuous training in project management, cross-cutting issues.An interesting and versatile workplace and a pleasant working atmosphere.Be part of an excellent multidisciplinary research centre with the HRS4R badge.
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