Overview
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.
Perfil del éxito
¿Posee estas competencias sociales y rasgos interpersonales para tener éxito en Parexel?
- Comunicador
- Organizado
- Contratos laborales flexibles
- Emprendedor
- Orientado al detalle
- Solucionador de problemas
Acerca de este rol
Job Summary:
The Senior Clinical Research Associate (Sr CRA) will be a member of the Monitoring team and provide monitoring expertise to individual clinical trials and/or programs.
Key Accountabilities:
Conduct and provide support for in-house and outsourced clinical site monitoring activities to ensure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs) and study protocols
Collaborate with study teams during start-up/feasibility and conduct site identification and assessment tasks.
Identify root causes and proactively escalate and resolve CRA and site performance issues through collaboration with stakeholders
Provide Monitoring expertise, mentoring and training to less experienced team members as required
Build positive working relationships and proactively seek feedback from site teams (e.g., Principal Investigators, Study Coordinators, Pharmacists, Site Administration)
Partner with study teams and sites in conducting site outreach activities, including patient recruitment and retention strategies
Provide input and lead cross-functional teams through the process to determine monitoring strategy (risk-based monitoring) for studies as required
Use regional knowledge to localize study processes and documents where possible
Represent Monitoring at Investigator Meetings as required
Perform other tasks as required
Required Knowledge, Skills, and Abilities:
5+ years monitoring experience in clinical research experience required (i.e., biotechnology, pharmaceutical, Contract Research Organization (CRO))
Oncology monitoring experience required
Travel as required, to include domestic and international
Demonstrates working knowledge of GCP, ICH guidelines and FDA regulations
Demonstrates ability to work independently and in a team environment
Proficiency with MS Office 365 (e.g., Word, Excel, PowerPoint, Outlook, SharePoint)
Excellent oral and written communication skills and strong organizational abilities
Education:
BA/BS, nursing degree, or advanced degree required. Degree in the life sciences preferred
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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
Perspectivas de los empleados
nuestro equipo
