Job Summary
The Clinical Research Associate (Site Director) plays a crucial role in overseeing clinical trials at selected sites, ensuring adherence to regulatory standards and the successful execution of research studies. This position entails acting as a liaison between stakeholders, managing site-specific operations, and facilitating compliance with protocols.
Responsibilities
- Oversee and manage the clinical trial operations at assigned study sites.
- Ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP).
- Develop and maintain strong relationships with site personnel and stakeholders, providing guidance and support throughout the study.
- Coordinate site visits, training sessions, and audits to enhance performance and resolve any issues that arise.
- Monitor patient recruitment and retention metrics, implementing strategies to optimize enrollment.
- Prepare and manage study-related documentation and reports, ensuring accurate data collection and reporting.
Qualifications
- Bachelor’s degree in life sciences or a related field; advanced degrees are a plus.
- Previous experience in clinical research or management of clinical trials.
- Strong understanding of regulatory requirements and clinical research methodology.
- Excellent communication and interpersonal skills essential for fostering site relationships.
- Ability to work independently and make critical decisions regarding study processes.
- Proficiency in data analysis and familiarity with clinical trial management systems.
Codera LLC 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.
