Our organization is seeking a seasoned Clinical Research Associate to oversee the quality and compliance of clinical trial sites. This role requires effective collaboration with internal and external stakeholders, as well as a deep understanding of clinical research processes.
Key Responsibilities:
* Lead clinical trial site operations and ensure adherence to regulatory guidelines
* Collaborate with cross-functional teams to drive process improvements and stakeholder engagement
* Maintain up-to-date knowledge of clinical research methodologies and industry trends
Requirements:
* Bachelor's degree in life sciences or related field
* Strong analytical and communication skills, with experience in clinical research coordination
* Minimum one year of experience in clinical research, with a focus on site management and operations