Principal Study Coordinator
hace 16 horas
Principal Study Coordinator – €35-€40k per annum – Home based, with travel to clinical sites as required (Barcelona, Spain)
The Role
Do you have experience as a clinical research coordinator, CRA and/or study coordinator? Do you thrive in innovative agile work environments? If so, VCTC Research is looking for a Principal Study Coordinator to join our newly establish clinical research centre in Barcelona.
As a key member of our clinical research team, you will ensure that our clinical trials run smoothly, efficiently, and in compliance with all regulatory requirements. You will report to the Managing Director with opportunities for career progression in a fast-growing organization.
Take the next step in your career with VCTC Research – apply now, we look forward to hearing from you
Key Responsibilities:
Project Planning and Execution: Develop comprehensive project plans, ensuring all activities are completed on time and within budget.
Team Coordination: Work closely with vendors, suppliers, and clinical site staff to facilitate trial operations.
Patient Coordination: Collaborate with Research Nurses and Patient Engagement Specialists to ensure a positive study experience for all participants.
Communication: Act as the primary point of contact with study monitors, providing regular updates on project status.
Regulatory Compliance: Ensure all activities align with Good Clinical Practice (GCP) and local regulations.
Documentation and Reporting: Maintain accurate records of all trial activities, including meeting minutes and progress reports.
Quality Control: Monitor trial quality and data collection processes to ensure compliance with protocols.
Training and Development: Provide training and guidance to clinical staff to uphold protocol standards.
The Company
VCTC Research is a patient centric clinical trial centre that eliminates the burden of participation and facilitates the rapid recruitment of patients. Our pioneering processes take clinical trials to our patients, providing access to all, generating diversity and quality data through a compassionate, expedited virtual clinical trial process.
At our core we enhance the clinical trial experience for participants and sponsors leading to expedited timelines, reduced cost and ultimately bringing products to market quicker.
This is, and always will be, a core part of VCTC Research.
The Person
Within one hour commute to Barcelona, Spain
Strong experience at a clinical trial or in a healthcare setting.
Successful track record of effectively managing studies.
Strong understanding of clinical trial processes, regulations, and best practices.
Excellent organisational, problem-solving, and multitasking skills.
Strong communication and interpersonal skills, with the ability to work effectively with diverse teams.
Full professional proficiency in Spanish and English required, and Catalan preferred.
Proficiency in project management software and tools.
Ability to work independently and manage multiple projects simultaneously.
Coordinador/a Principal de Estudio – €35-€40k anuales – Trabajo desde casa, con viajes a sitios clínicos según sea necesario (Barcelona, España)
El puesto
¿Tienes experiencia como coordinador/a de investigación clínica, CRA y/o coordinador/a de estudios? ¿Te desenvuelves bien en entornos de trabajo ágiles e innovadores? Si es así, VCTC Resecar está buscando un/a Coordinador/a Principal de Estudio para unirse a nuestro recién establecido centro de investigación clínica en Barcelona.
Como miembro clave de nuestro equipo de investigación clínica, garantizarás que nuestros ensayos clínicos se realicen de manera fluida, eficiente y en cumplimiento con todos los requisitos normativos. Reportarás directamente al director general, con oportunidades de desarrollo profesional en una organización en rápido crecimiento.
Da el siguiente paso en tu carrera con VCTC Resecar: aplica ahora, esperamos saber de ti
Responsabilidades clave:
Planificación y Ejecución de Proyectos: Desarrollar planes de proyecto integrales, asegurando que todas las actividades se completen a tiempo y dentro del presupuesto.
Coordinación del Equipo: Trabajar estrechamente con proveedores, suministradores y personal de los sitios clínicos para facilitar las operaciones de los ensayos.
Coordinación de Pacientes: Colaborar con Enfermeras de Investigación y Especialistas en Compromiso del Paciente para asegurar una experiencia de estudio positiva para todos los participantes.
Comunicación: Actuar como el principal punto de contacto con los monitores de estudio, proporcionando actualizaciones regulares sobre el estado del proyecto.
Cumplimiento Normativo: Asegurar que todas las actividades se alineen con las Buenas Prácticas Clínicas (BPC) y las normativas locales.
Documentación e Informes: Mantener registros precisos de todas las actividades del ensayo, incluyendo actas de reuniones e informes de progreso.
Control de Calidad: Supervisar la calidad del ensayo y los procesos de recopilación de datos para asegurar el cumplimiento de los protocolos.
Formación y Desarrollo: Proporcionar formación y orientación al personal clínico para mantener los estándares del protocolo.
La Empresa
VCTC Resecar es un centro de ensayos clínicos centrado en el paciente, que elimina las barreras de participación y facilita el rápido reclutamiento de pacientes. Nuestros procesos pioneros llevan los ensayos clínicos directamente a los pacientes, proporcionando acceso a todos, generando datos diversos y de calidad a través de un proceso compasivo y acelerado de ensayos clínicos virtuales.
En nuestro núcleo, mejoramos la experiencia de los ensayos clínicos para los participantes y patrocinadores, lo que lleva a plazos más rápidos, costes reducidos y, en última instancia, a llevar los productos al mercado más rápidamente.
Esto es, y siempre será, una parte fundamental de VCTC Resecar.
La Persona
Residir a una hora de Barcelona, España.
Amplia experiencia en un sitio de ensayo clínico o en un entorno sanitario.
Historial demostrado de gestionar eficazmente estudios.
Sólido conocimiento de los procesos, normativas y mejores prácticas de ensayos clínicos.
Excelentes habilidades organizativas, de resolución de problemas y de multitarea.
Fuertes habilidades de comunicación e interpersonales, con la capacidad de trabajar eficazmente con equipos diversos.
Dominio profesional completo del español y el inglés, y se prefiere catalán.
Competencia en software y herramientas de gestión de proyectos.
Capacidad para trabajar de manera independiente y gestionar múltiples proyectos simultáneamente
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