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Research Coordinator
3 months ago
**Job Summary**
**Must have 3 consecutive years recent experience in a trial study**
**Responsibilities**
- Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
- Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;
- Attend all relevant study meetings;
- Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
- Design and maintain source documentation based on protocol requirements;
- Schedule and execute study visits and perform study procedures;
- Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics;
- Participate in “huddles” to confirm daily study tasks are assigned to team members and are executed to the expected standards;
- Assist with study data quality checking and query resolution.
**Qualifications**
- **Must have 3 consecutive years recent experience in a trial study**:
- Phlebotomy experience / certification preferred
- Spanish Speaking / Bilingual preferred
