Logopeda En Badalona

Cronoshare.Com

Badalona

Remote

EUR 32,000 - 52,000

Full time

40 hours ago
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Benefits offered by this job

Remote work from home
Flexible schedule
Professional development

Job summary

Cronoshare.Com busca un logopeda infantil altamente cualificado para sesiones 100% remotas, orientado a niños de 0 a 6 años. Trabajarás desde casa, evaluando, diagnosticando e interviniendo con planes personalizados y colaborando con familias para optimizar el desarrollo del lenguaje.

Se valorará experiencia en teleterapia y manejo de herramientas digitales, con título oficial y habilitación profesional. Contrato a jornada completa y horario flexible.

Qualifications

  • Máster o especialización en Logopedia Infantil o Trastornos del Lenguaje.
  • Título universitario en Logopedia o Terapia del Lenguaje.
  • Experiencia mínima demostrable de 3 años en logopedia infantil.
  • Conocimiento de plataformas de teleterapia y herramientas digitales.

Responsibilities

  • Realizar evaluaciones del lenguaje, habla y comunicación en niños 0–6 años mediante teleterapia.
  • Diseñar e implementar planes de intervención logopédica personalizados.
  • Impartir sesiones en plataformas online interactivas.
  • Asesorar a padres y cuidadores con estrategias para el hogar.
  • Mantener registros de evaluaciones, tratamientos y progreso.
  • Colaborar con otros profesionales para un enfoque integral.

Job description

About the Role Estamos buscando un/a Logopeda altamente cualificado/a y con experiencia en el ámbito infantil para unirse a nuestro equipo en modalidad 100% remota. El/la candidato/a ideal se especializará en la evaluación, diagnóstico e intervención de trastornos del lenguaje, habla y comunicación en niños de 0 a 6 años. Trabajarás directamente desde casa, utilizando plataformas de teleterapia para ofrecer sesiones de alta calidad y apoyo a las familias. Buscamos a un/a profesional comprometido/a con la mejora de la comunicación de los más pequeños y con gran habilidad para adaptarse a las herramientas digitales, contribuyendo a nuestro servicio en expansión. Key Responsibilities

  • Realizar evaluaciones completas del lenguaje, habla y comunicación en niños a través de herramientas de teleterapia.
  • Diseñar e implementar planes de intervención logopédica personalizados, adaptados a las necesidades individuales de cada niño.
  • Impartir sesiones de terapia de lenguaje, habla y comunicación utilizando plataformas online interactivas y recursos digitales.
  • Ofrecer asesoramiento y apoyo a los padres y cuidadores, enseñándoles estrategias para fomentar el desarrollo del lenguaje en el hogar.
  • Mantener registros detallados de las evaluaciones, planes de tratamiento y progreso de los pacientes.
  • Colaborar con otros profesionales de la salud y la educación (si es necesario) para asegurar un enfoque integral en la atención al niño.
  • Mantenerse actualizado/a sobre las últimas investigaciones, técnicas y tecnologías en logopedia y teleterapia infantil.
  • Garantizar la confidencialidad y seguridad de la información del paciente en todo momento.
Requirements
  • Título universitario en Logopedia o Terapia del Lenguaje.
  • Máster o especialización en Logopedia Infantil o Trastornos del Lenguaje.
  • Experiencia mínima demostrable de 3 años trabajando como logopeda con niños, preferiblemente en la etapa de educación infantil.
  • Conocimiento profundo de los diferentes trastornos del lenguaje (receptivo, expresivo, de articulación, fluidez, voz) y sus abordajes terapéuticos.
  • Experiencia o gran disposición para utilizar plataformas de teleterapia y herramientas digitales de forma efectiva.
  • Excelentes habilidades de comunicación, empatía y capacidad para crear un ambiente terapéutico positivo a distancia.
  • Habilidad para motivar a los niños y a sus familias a través de la pantalla.
  • Certificado de habilitación profesional para ejercer la logopedia.
  • Se valorará experiencia en el uso de software específico para logopedia y creación de materiales interactivos.
  • Se requiere un espacio de trabajo tranquilo y privado, conexión a internet de alta velocidad y equipo informático fiable.
Benefits Ofrecemos un contrato a jornada completa con un salario competitivo, acorde a la experiencia y especialización. Esta es una oportunidad única para trabajar de forma remota desde cualquier ubicación, brindando servicios esenciales de logopedia. Formación continua en teleterapia y nuevas metodologías. Horario flexible que permite una mejor conciliación de la vida personal y profesional. Ser parte de un equipo innovador y dedicado a mejorar la comunicación y el desarrollo infantil. Potencial de crecimiento dentro de la organización a medida que expandimos nuestros servicios.

Our client is seeking an exceptional and experienced Logopeda Infantil with a specialization in speech and language disorders to join their fully remote therapeutic team. This role is critical in providing essential speech and language therapy services to young children across various locations, all conducted virtually. You will assess, diagnose, and treat communication and swallowing disorders, working closely with families to develop and implement personalized intervention plans. This position offers the unique advantage of working from home, allowing for significant flexibility and work-life balance.

About the Role
Our client is seeking an exceptional and experienced Logopeda Infantil with a specialization in speech and language disorders to join their fully remote therapeutic team. This role is critical in providing essential speech and language therapy services to young children across various locations, all conducted virtually. You will assess, diagnose, and treat communication and swallowing disorders, working closely with families to develop and implement personalized intervention plans. This position offers the unique advantage of working from home, allowing for significant flexibility and work-life balance.
Key Responsibilities

  • Conduct comprehensive remote assessments of speech, language, communication, and swallowing disorders in children.
  • Develop and implement individualized tele-therapy treatment plans tailored to each child's needs.
  • Deliver engaging and effective speech and language therapy sessions via secure video conferencing platforms.
  • Provide guidance and training to parents and caregivers on how to support their child's communication development at home.
  • Monitor and document children's progress, adjusting treatment plans as needed.
  • Collaborate with other healthcare professionals and educators remotely to ensure a holistic approach to child development.
  • Maintain accurate and confidential electronic client records in compliance with data protection regulations.
  • Stay up-to-date with the latest advancements and best practices in pediatric speech-language pathology and tele-therapy.
  • Utilize a variety of digital tools and resources to enhance therapy sessions.
  • Advocate for the communication needs of children within their families and communities.
Requirements
  • Master's degree in Speech-Language Pathology (Logopedia) from an accredited institution.
  • Current and valid license or certification to practice speech-language pathology in Spain.
  • Minimum of 4 years of clinical experience working specifically with children with speech and language impairments.
  • Proven experience and comfort delivering tele-therapy services.
  • In-depth knowledge of various communication disorders (e.g., articulation disorders, language delays, fluency disorders, voice disorders, feeding/swallowing issues).
  • Excellent virtual communication, interpersonal, and motivational skills.
  • Proficiency in using tele-therapy platforms, EMR systems, and other relevant digital technologies.
  • Strong organizational skills and the ability to manage a remote caseload effectively.
  • Fluency in Spanish; proficiency in English is a strong asset.
  • Commitment to providing high-quality, evidence-based care.
Benefits

This position offers a competitive salary, the immense benefit of a fully remote work arrangement, and opportunities for professional development in the field of tele-rehabilitation. You will be part of a supportive, forward-thinking team dedicated to improving children's lives from the convenience of your home office. This is an excellent opportunity to advance your career in pediatric speech-language pathology.

Athens, Greece
Lisbon, Portugal
Brussels, Brussels-Capital Region, Belgium
Belgrade, Serbia
Barcelona, Spain
London, United Kingdom
Madrid, Spain
Full time
R
The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator's Brochures (IBs) and IB updates, Biomarker Reports, and submission documents such as the Summary of Clinical Efficacy and Safety, etc. Emphasis will be placed on the therapeutic areas of eye health and inflammation; senior-level experience in this areas is preferred.
The FTE Medical Writer will work on a dedicated basis and be embedded in sponsor's processes and workflows, including Feedback and Alignment Meetings. In this role, the FTE Medical Writer will participate in ongoing project-related activities, such as planning, project discussions, and all required training sessions. The FTE Medical Writer will adopt sponsor's systems, tools, and methodologies to ensure seamless collaboration and alignment with internal teams.
Tasks typically include, but are not limited to:
+ Document management: Set-up and management of clinical document in the Electronic Document Management System (EDMS)
+ Review and approval of the Statistical Analysis Plan in the EDMS
+ Management of timelines including proposal of timelines to trial/project team (based on timelines communicated by sponsor), finalising them after agreement, and updating them as appropriate
+ Preparation for and attendance of the required trial team meetings or submission meetings
+ Preparation, conduct, and documentation of kick-off meetings, e.g. for TDO/CTP, IB or CTR writing
+ Preparation, conduct, and documentation of Results Alignment Meetings (RAM; not applicable for Phase I in healthy volunteer studies)
+ Writing of drafts including appropriate in-text tables and figures according to the timelines agreed upon with trial/project team
+ Provision of drafts and management of all review cycles by the trial/project team, reaching consensus on comments/changes, integration of changes into the text, and completion of the Review Documentation Form (as applicable)
+ Initiation and monitoring or conducting of Quality Control (QC) checks as well as completion of the Quality Control Documentation Form (QCDF)
+ Creation and provision of the final document version to the trial/project team
+ Initiation of publishing and pre-archive checks, monitoring and resolution of findings
+ E-approval of final clinical document in the EDMS
+ Technical checks after the final draft of initial IBs and IB updates in the EDMS, and by going through a Final Formatting checklist document
+ FTE Medical Writer will follow the appropriate process as per document type and according to sponsor SOPs
Qualifications
+ Bachelor's degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred
+ Approx 5 years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be considered
+ Strong knowledge of global regulatory requirements and guidelines (e.g., ICH, FDA, EMA) across all phases of clinical development
+ Broad understanding of clinical research processes, including study design, data analysis, and regulatory submission requirements
+ Demonstrated ability to lead writing activities for complex documents and provide strategic input to cross-functional teams
+ Excellent written and verbal communication skills, with the ability to clearly and accurately present complex scientific and clinical information
+ Strong organizational, time management, and project management skills, with the ability to manage multiple priorities and meet tight deadlines
+ Proven ability to work collaboratively in a cross-functional, team-oriented environment while also operating independently when needed
+ High attention to detail with a commitment to quality, consistency, and scientific accuracy
+ Proficiency in Microsoft Word and document formatting best practices
+ Experience with electronic document management systems (eDMS) and familiarity with document templates, style guides, and structured authoring tools
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

London, United Kingdom
Amsterdam, Netherlands
Porto Salvo, Portugal
Mannheim, Baden-Württemberg, Germany
Dublin, Ireland
Illkirch-Graffenstaden, France
Bordeaux, France
Köln, North Rhine-Westphalia, Germany
Tel Aviv, Israel
Munchen, Bavaria, Germany
Edinburgh, Scotland, United Kingdom
Madrid, Spain
Athens, Greece
Frankfurt, Hesse, Germany
Barcelona, Spain
Zurich, Switzerland
Gothenburg, Sweden
Full time
R
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.
The Patient Centered Solutions team (PCS) The PCS team leads the industry in the science of measuring the patient experience. We pair strategic consulting expertise with technical scientific knowledge to design and execute scientifically rigorous research that incorporates the patient voice into the development and commercialization of new medicines. This research includes qualitative (e.g., patient interviews, focus groups), quantitative (clinical outcome assessments (COAs)/patient-reported outcomes (PROs), preference research), and passive (digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment.
Why join?
+ Become part of a recognized global leader in patient-focused research
+ Keep growing with an organization that encourages and invests in continuous professional and personal development
+ Apply your business and leadership skills in an entrepreneurial and multi-disciplinary team
+ Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry
+ Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient-centric
Responsibilities
The Associate Principal/ Principal Clinical Outcome Assessment (COA) Endpoint Strategy serves as the subject matter expert for COA endpoint strategy, ..." (truncated to fit)

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