MarlexMarlex es una empresa líder en Recursos Humanos especializada en Selección de Personal.Contamos con más de 25 años de experiencia en el sector y una red de más de 60 oficinas, posicionándonos como una de las 5 firmas del país líderes a nivel peninsular y una de las de más alto crecimiento en los últimos años.Compartimos viaje con más de 5.000 empresas que confían en nuestros servicios y equipos especializados.Descripción de la ofertaFrom Marlex Great People, we are searching a Clinical Project Manager to work in an important pharmaceutical laboratory, with their headquarters in BarcelonaWhat responsibilities will you have?Lead and manage a multidisciplinary clinical trial team, ensuring effective planning, evaluation and implementation of assigned clinical studies and programsCollaborate with colleague/investigator team to establish realistic project timelines and escalate any unresolved issues to higher managementOrganize and facilitate investigators meetings and internal meetings related to study execution and operational excellenceInteract with investigation sites and CRAs/CROs/vendors to ensure appropriate study setup and conductMonitor site performance, review site visit reports and monitor activities of quality controlAssist in developing and review of study documentation; study protocol, IB, treatment plans,



informed consent forms and other essential study documentsSupport compilation of study regulatory documents for submission and communication with internal/external stakeholdersReview of medical/scientific data quality, coordinate data analysis and interpretation of resultsInteract with medical writer to ensure completion of Clinical Study Report (CSR)Setup and maintain Trial Master File (TMF), Clinical Trial Management System (CTMS) in collaboration with colleagues/vendorsWhat do we offer?The option to be a part of a growing company, in which you’ll be able to develop your professional career.Permanent contractPartial remote workRequisitosDegree in Life science.3+ years of clinical operations experience with strong management experience in planning, driving, reporting, and publishing clinical studies (interventional, observational, early to late phases).Previous experience in a pharmaceutical company/CRO is highly desirable.Thorough knowledge of Good Clinical Practices (GCPs), clinical study design, regulatory processes, and general clinical development process.Knowledge of basic statistics and good skills in Microsoft officeHigh English level (oral and written)Ability to work independently and lead multidisciplinary cross-functional teamUbicación: Barcelona (España)Tipo de Contrato: IndefinidoJornada laboral: Jornada completaSector: Farmacéutico y biotecnología Vacantes: 1Disciplina: I+DModalidad de trabajo: Híbrida

📌 Clinical Project Manager (Pharma) (Barcelona)
🏢 Marlex Human Capital
📍 Barcelona