Site Activation Partner
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Job Description
Site Activation Partner optimizing clinical trial site operations and managing compliance in Brazil. Leading activities from startup to closeout for assigned studies in clinical research.
Responsibilities:
- Lead or support operational activities from start up to close out for assigned studies
- Coordinate activities and document management during start up towards high quality Investigator Initiation Package
- Prepare and submit regulatory documents for internal approval
- Manage timely communication and documentation between client and central ethics committees
- Ensure maintenance of IRB/Ethics activities and timely filing of documents
Requirements:
- Minimum 2 years relevant experience in clinical site management
- Knowledge of clinical trial methodologies
- Understanding of ICH/GCP and FDA regulations
- Must be fluent in local language and in English
- Good technical skills and ability to learn multiple systems
Benefits:
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
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