Clinical Research Specialist
2 weeks ago
This is an exciting opportunity to work in a dynamic environment as a Study Coordinator.
We are seeking a highly organized and skilled professional with at least 1 year of clinical research experience to join our team.
The ideal candidate will be responsible for reporting adverse events, data entry, administrative tasks, and query resolution on a daily basis.
Key Responsibilities:
- Reporting adverse events
- Data entry and management
- Administrative tasks
- Query resolution
Requirements:
- Oncology experience
- Strong understanding of complex medical concepts
- Excellent computer skills
Salary and Benefits:
The estimated salary for this position is $62,500 - $82,500 per year, depending on location and qualifications. Additional benefits include competitive compensation packages and opportunities for growth and development.
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