Clinical Study Manager

2 semanas atrás

Belo Horizonte, Brasil beBeeClinicalResearch Tempo inteiro

Job Opportunity: We are currently seeking a detail-oriented and experienced Clinical Research Associate (CRA) to oversee and manage clinical trials for Phase 2 Seizure studies. Site Oversight and Monitoring: The selected individual will be responsible for conducting site qualification, initiation, interim monitoring, and close-out visits. Ensuring proper adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements at the designated sites. Key Responsibilities Include: Regulatory Compliance: Reviewing informed consent documents and confirming appropriate consenting procedures. Required Qualifications: Bachelor's degree in Life Sciences, Nursing, or a related field is required. A minimum of 2-4 years of experience as a Clinical Research Associate in oncology trials, with a preference for Phase 2 experience. Preferred Qualifications: Previous experience in early-phase oncology trials, such as dose escalation studies and first-in-human trials. Why You Should Apply: This role presents an excellent opportunity to develop your skills and expertise in clinical research while working on a challenging project.

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