Job Summary
The role of Clinical Research Associate II involves overseeing and supporting clinical trials to ensure compliance with regulatory standards and protocols. This position works collaboratively to monitor the progress of clinical studies, ensuring data accuracy and participant welfare throughout the research process.
Responsibilities
- Conduct site visits and monitor clinical trial sites to evaluate trial progress and adherence to protocols.
- Review and verify data collection processes to uphold data integrity and regulatory compliance.
- Collaborate with investigators and site personnel to facilitate smooth operational flow and resolve any issues that arise.
- Prepare and maintain essential study documentation including trial protocols, informed consent forms, and regulatory submissions.
- Support training for site staff on clinical trial requirements and provide ongoing guidance.
- Participate in data analysis and contribute to study reports and presentations.
Qualifications
- Bachelor’s degree in a relevant scientific field or equivalent experience.
- A minimum of two years’ experience in clinical research, preferably as a Clinical Research Associate.
- In-depth knowledge of Good Clinical Practice (GCP) and relevant regulatory requirements.
- Strong organizational skills and attention to detail to manage multiple tasks effectively.
- Excellent communication and interpersonal skills to work collaboratively with different stakeholders.
- Proficiency in clinical trial management software and Microsoft Office Suite.
City of Hope 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.
