
Clinical Research Project Coordinator
Há 7 horas
Parexel is seeking multiple Site Activation Partners in Brazil. The SAP leads or supports operational activities from start-up to close-out, ensuring compliance with study timelines and laws, Good Clinical Practices, and Client standards.
Key Responsibilities:- Clinical Trial Site Activation: Initiate and coordinate site activation activities, register investigator sites, and manage documents.
- Clinical Trials Conduct: Post-activation, initiate and coordinate activities, ensure IRB/Ethics maintenance, and timely filing of documents.
- Internal & External Communication: Maintain ongoing contact with the study team, respond to requests, and disseminate information.
- Clinical Trial Site Support: Perform awareness sessions, resolve issues, and align with study teams on corrective actions.
- Minimum 2 years' experience in clinical site management.
- Knowledge of clinical trial methodologies, ICH/GCP, FDA, and Global/local country regulations.
- Effective communication skills and technical ability to learn multiple systems.
- Demonstrated knowledge of clinical research processes and quality expectations.
Opportunities for career growth and professional development.
About This Role:This role involves supporting the initiation and coordination of site activation activities, managing documents, and maintaining ongoing contact with the study team.
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