Job Summary
The Clinical Research Associate II will be part of CTI Clinical Trial and Consulting Services, a clinical contract research organization (CRO) in the United States. This role involves engaging with investigators, clients, and project teams to oversee and support clinical trials while ensuring compliance with industry standards.
Responsibilities
- Collaborate with investigators and project teams on various clinical trial phases.
- Monitor trial processes to ensure adherence to protocols and regulatory requirements.
- Evaluate data integrity and documentation within clinical research projects.
Qualifications
- Education in nursing, pharmacy, health or natural sciences, or an Associate’s Degree with relevant experience.
- At least three years of nursing experience or comparable clinical trial experience.
- Strong understanding of clinical research regulations and best practices.
CTI provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
