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Clinical Research Associate II
About the Role:- Assume primary responsibility for assigned study sites, ensuring seamless monitoring and delivery of project goals.
- Conduct site visits and complete related deliverables with quality and adherence to timelines, regulatory requirements, SOPs, and ICH GCP guidelines.
- Support study start-up activities, including feasibility assessments, pre-study preparations, and site selection.
- Collect, review, and track essential and regulatory documents, ensuring accuracy and compliance.
- Pursue ongoing professional development through required training and education, enhancing skills and expertise in clinical research monitoring.
- A minimum of 3 years of clinical trial monitoring experience or equivalent experience as determined by management and HR.
- Fluency in English is mandatory; proficiency in Spanish is considered an asset.
- Bachelor's Degree or higher in an allied health field such as nursing, pharmacy, or health/natural science, or RN with Associate's Degree, or 3-year Nursing Diploma with at least 2 years of clinical nursing experience.
- Previous experience in conducting clinical research studies in a hospital setting, pharmaceutical company, or CRO.
- Fully eligible to work in Brazil, with no visa sponsorship provided.
- An office-based setting in São Paulo, providing a unique opportunity to collaborate with colleagues and contribute to cutting-edge research projects.
This role requires a high degree of autonomy, adaptability, and attention to detail. If you are a motivated and organized individual with a passion for clinical research, we encourage you to apply.
