Técnico De Biobanco Para Investigación Clínica

Agencia De Vivienda Y Rehabilitacion De Andalucia; Málaga; Remote; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Remote work

Professional development opportunities

Job summary

Our client, a leading global pharmaceutical research organization, seeks a highly motivated Pharmacist to join their expanding clinical research division in a fully remote role. Ideally based in Granada or nearby, you will design, implement, and monitor trials with international teams.

You will ensure data integrity, master GCP and regulatory standards, and collaborate with investigators, sites, and regulators. Fluent in Spanish and English, you will manage study documents from home.

Qualifications

• Master's or Doctoral degree in Pharmacy or life sciences.
• At least 5 years in clinical research or related pharma field.
• Knowledge of GCP and regulatory affairs (FDA/EMA) and data capture systems.

Responsibilities

• Oversee and manage clinical trials ensuring GCP compliance and regulatory requirements.
• Collaborate with investigators and site staff for trial execution and patient safety.
• Review and interpret trial data, identify issues and propose solutions.
• Develop study protocols, informed consent forms, and essential documents.
• Manage drug accountability and storage/dispensing of investigational products.
• Act as a point of contact for study sites and queries.
• Participate in site selection, initiation, monitoring, and close-out visits (remote when possible).
• Contribute to analysis and reporting of trial results.
• Stay updated on developments in pharmaceutical research and regulatory affairs.

Skills

Analytical skills

Problem-solving

Organization

Bilingual communication

Regulatory knowledge

Remote work

Attention to detail

Education

Pharmacy degree

Tools

EDC systems

CTMS

Job description

About the Role

Our client, a leading global pharmaceutical research organization, is seeking a highly motivated and experienced Farmacéutico/a to join their expanding clinical research division. This is a fully remote position, allowing you to contribute from the comfort of your home, ideally based in or near Granada, Andalusia . You will play a pivotal role in the design, implementation, and monitoring of clinical trials, ensuring data integrity and adherence to regulatory standards. This role requires a deep understanding of drug development processes and a passion for advancing medical science. You will work collaboratively with a diverse, international team of researchers, clinicians, and regulatory specialists. The opportunity provides unparalleled flexibility and the chance to impact groundbreaking medical advancements from anywhere.

About the Role

Our client, a leading global pharmaceutical research organization, is seeking a highly motivated and experienced Farmacéutico/a to join their expanding clinical research division. This is a fully remote position, allowing you to contribute from the comfort of your home, ideally based in or near Granada, Andalusia . You will play a pivotal role in the design, implementation, and monitoring of clinical trials, ensuring data integrity and adherence to regulatory standards. This role requires a deep understanding of drug development processes and a passion for advancing medical science. You will work collaboratively with a diverse, international team of researchers, clinicians, and regulatory specialists. The opportunity provides unparalleled flexibility and the chance to impact groundbreaking medical advancements from anywhere.

Key Responsibilities

• Oversee and manage various aspects of clinical trials, ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Collaborate with investigators and site staff to ensure smooth trial execution and patient safety.
• Review and interpret clinical trial data, identifying potential issues and proposing solutions.
• Develop and finalize study protocols, informed consent forms, and other essential trial documents.
• Manage drug accountability and ensure proper storage and dispensing of investigational products.
• Act as a key point of contact for study sites, addressing queries and providing support.
• Participate in site selection, initiation, monitoring, and close-out visits (remotely where possible).
• Contribute to the analysis and reporting of clinical trial results.
• Stay updated on the latest developments in pharmaceutical research and regulatory affairs.

Requirements

• Master's or Doctoral degree in Pharmacy (Farmacia) or a related life science field.
• Minimum of 5 years of experience in clinical research, pharmaceutical industry, or a related area.
• In-depth knowledge of clinical trial phases, study design, and regulatory affairs (FDA, EMA, etc.).
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent analytical, problem-solving, and organizational skills.
• Strong written and verbal communication skills in Spanish and English.
• Ability to work independently, manage multiple priorities, and meet deadlines in a remote setting.
• Detail-oriented with a strong commitment to quality and compliance.
• Understanding of GCP guidelines is essential.

Benefits

This fully remote position offers a highly competitive salary and the flexibility to work from home. Our client provides excellent professional development opportunities, including access to specialized training and conferences. You will be part of an innovative and dynamic global team, contributing to life-changing medical research. While remote, our client fosters a strong sense of community through virtual interactions and team-building activities. This role is ideal for a self-disciplined professional seeking a challenging and rewarding career in pharmaceutical research without geographical constraints.

About the Role

Nuestro cliente, una destacada empresa farmacéutica en expansión, busca incorporar a su equipo un/a Farmacéutico/a Especialista en Investigación Clínica. Esta posición es completamente remota, brindando una flexibilidad excepcional para profesionales que desean contribuir desde cualquier ubicación. El/la candidato/a seleccionado/a será fundamental en el diseño, implementación y seguimiento de estudios clínicos, asegurando el cumplimiento de las normativas y los más altos estándares de calidad. Buscamos a una persona proactiva, con una sólida base científica y una gran capacidad para la gestión de proyectos. El entorno de trabajo es dinámico e innovador, fomentando el desarrollo profesional continuo y la colaboración interdisciplinaria. Esta oportunidad representa un paso clave en la carrera de un farmacéutico con interés en el ámbito de la investigación y el desarrollo de nuevos medicamentos, con la ventaja de un modelo de trabajo 100% remoto, que permite conciliar la vida personal y profesional de manera óptima. Se valorará la experiencia previa en el sector farmacéutico y en entornos de investigación.

Key Responsibilities

• Coordinar y supervisar la ejecución de ensayos clínicos, desde la fase de diseño hasta el cierre del estudio.
• Garantizar el cumplimiento de los protocolos de investigación, las Buenas Prácticas Clínicas (BPC/GCP) y la legislación vigente.
• Gestionar la relación con los centros de investigación, investigadores y otros stakeholders del estudio.
• Supervisar la recopilación, validación y análisis de datos clínicos.
• Identificar y evaluar posibles riesgos en el desarrollo del ensayo y proponer medidas correctivas.
• Preparar y presentar informes de progreso y resultados de los estudios clínicos.
• Participar en la elaboración de planes de investigación y la selección de nuevos proyectos.
• Mantenerse actualizado/a sobre los avances científicos y tecnológicos en el campo de la investigación clínica.
• Colaborar estrechamente con los equipos de desarrollo de producto, regulación y farmacovigilancia.

Requirements

• Título de Farmacia o equivalente, con colegiación activa.
• Experiencia demostrable en investigación clínica, preferiblemente en la industria farmacéutica.
• Conocimiento profundo de las normativas BPC/GCP y legislación farmacéutica aplicable.
• Habilidades sólidas en gestión de proyectos, planificación y organización.
• Capacidad para trabajar de forma autónoma y en equipos multidisciplinares, de forma remota.
• Excelentes habilidades de comunicación verbal y escrita en español.
• Dominio de herramientas informáticas, incluyendo software de gestión de datos clínicos.
• Proactividad, pensamiento crítico y orientación a resultados.
• Se valorará positivamente un Máster o especialización en Investigación Clínica o Farmacología.
• Experiencia en la monitorización de ensayos clínicos es un plus.

Benefits

• Contrato indefinido con un salario competitivo acorde a la experiencia.
• Oportunidad de trabajar de forma 100% remota, sin necesidad de desplazamientos.
• Participación en proyectos innovadores y de alto impacto en el sector farmacéutico.
• Desarrollo profesional continuo a través de formación y asistencia a congresos.
• Excelente ambiente de trabajo colaborativo y enfocado en la excelencia científica.
• Posibilidad de crecimiento dentro de una empresa líder en su sector.
• Herramientas de trabajo y soporte tecnológico para el desempeño remoto.