Site Management Associate
New
BrazilFull-TimeEntry
Salary not disclosed
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Job Details
- Required Skills
- GCPDocumentationData entry
Requirements
- Bachelor’s degree in Life Sciences, Healthcare Administration, Clinical Research, or related field
- Some experience in clinical research, site coordination, or administrative healthcare roles is preferred but not mandatory
- Basic understanding of clinical trial processes and regulatory frameworks such as GCP (preferred)
- Strong organizational skills with ability to manage multiple tasks and deadlines
- Excellent attention to detail and accuracy in documentation and data handling
- Strong communication and interpersonal skills for effective collaboration
- Ability to work in a team-oriented and fast-paced environment
- Proactive mindset with willingness to learn and develop in clinical operations
Responsibilities
- Assist in the monitoring of clinical trial sites to ensure compliance with protocols, GCP, and regulatory standards
- Support site management activities, including documentation preparation, data entry, and tracking of site performance metrics
- Collaborate with cross-functional clinical teams to address site-related issues and ensure smooth operations
- Maintain accurate and up-to-date records of site activities and contribute to monitoring reports
- Support communication between internal teams and external site stakeholders
- Participate in training and development activities to strengthen clinical research knowledge and skills
- Ensure operational consistency and data quality across assigned clinical trial sites
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