Job Description
O que buscamos:
- Complete higher education in Pharmacy, Biomedicine, or Nursing;
- Good Practices in Clinical Research, Initiation Visit, Routine, Close Out, and center qualification;
- Intermediate English;
- Minimum of 2 years experience in clinical research as a clinical research analyst, or previous experience as a research center coordinator.
Contamos com você para:
- General On-Site Monitoring Responsibilities, including routine monitoring visits and close-out of clinical sites;
- Conduct pre-study visits such as SQV Site Qualification Visit and SIV Site Initiation Visits;
- Ensure the integrity of the data submitted on Case Report Forms (CRFs) by carefully reviewing source documents;
- Perform CRF review, including generating and resolving queries, to ensure data quality;
- Maintain study files, ensuring audit readiness at the site level;
- Prepare...