Site Monitoring Lead (FSP) Inflammation Trials
Primary Location: Germany, Remote ID de la oferta R0000036495 Categoría Clinical Trials Fecha de publicación 11/04/2025Overview
Como Auxiliar de investigación clínica (CRA) en Parexel, usted cumple una función vital para hacerles llegar los tratamientos a los pacientes con mayor rapidez. La prioridad de nuestros CRA es la seguridad y el bienestar de los pacientes. Cuando viaje a centros de investigación y cumpla sus obligaciones de monitoreo, lo alentamos a ser inquisitivo, a asumir responsabilidades, a construir relaciones y a actuar con integridad.
Únase a un equipo con una gran variedad de experiencias y conocimientos y trabaje en proyectos globales dentro de una amplia gama de áreas terapéuticas. Estamos buscando personas que deseen crecer en el ámbito personal y profesional y que respalden a sus colegas de manera global y multidisciplinaria.
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Acerca de este rol
Parexel FSP has a new opening within our FSP Clinical Operations Team in Germany for a Site Monitoring Lead.
This roles is dedicated to a single sponsor and will support the Experimental Medicine (Early Clinical Trials) team, focusing on Inflammation studies.
About the Sponsor
Our sponsor is a leading biopharmaceutical company, recognized as one of the industry’s top investors in research and development. With a strong presence in both human and animal health, the company is committed to developing innovative therapies that address areas of high unmet medical need. Founded in Germany in 1885, the organization has remained independent and continues to improve and extend lives worldwide.
About the role:
Lead risk-based site monitoring strategies
Oversee CRO partners to ensure GCP and regulatory compliance
Provide expert guidance to CT Managers and CRAs
Contribute to trial planning, conduct, and close-out
Drive quality, training, and communication across global teams
Knowledge and Experience:
Substantial Site Management or CRA Lead experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Specifically within inflammation trials.
Demonstrated scientific and therapeutic knowledge and operational expertise across all Site Monitoring aspects in clinical trial planning and execution.
Understand dimensions of trial complexity include protocol, patients, sites, countries, vendors.
Ability to prioritize multiple tasks, and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise.
Education:
University (e.g., bachelor’s or comparable degree) in life sciences or related field OR several years of equivalent professional education may be acceptable if complemented by solid knowledge in and experience with Site Monitoring and Site Management processes and accountabilities.
Why Join Us?
This is an opportunity to work on cutting-edge early-phase trials with a sponsor that values innovation and collaboration. You’ll be part of a high-performing team making a real impact in areas of unmet medical need.
Apply Today
Take the next step in your career and join a team that’s shaping the future of clinical research
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POTENCIAL TRAYECTORIA PROFESIONAL
Parexel ofrece diversas trayectorias profesionales y programas de desarrollo interno para que los CRA avancen al próximo nivel. Esto podría incluir mejorar su puesto técnico, transferencia a gerencia o cambiar a otras áreas del negocio.
- APEX CRA
- CRA I
- CRA II
- CRA Sénior
- Gestión de ProyectosExperto en la MateriaGestión de Proyectos
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