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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.
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
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
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
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)