Job Summary
The Clinical Research Associate – Clinical Monitor role at the academic research institute in San Diego focuses on managing clinical trials aimed at addressing disease challenges. The position requires oversight of clinical study sites to ensure compliance and accurate data collection.
Responsibilities
- Monitor clinical trial sites to ensure adherence to protocols and regulatory requirements.
- Review Investigator Site Files to assure completeness and accuracy.
- Assess study data for integrity and compliance with established criteria.
- Collaborate with clinical teams to facilitate efficient trial conduct.
Qualifications
- Experience in clinical trial monitoring and research methodologies.
- Strong understanding of regulatory guidelines and compliance standards in clinical research.
- Excellent organizational and communication skills.
- Ability to work independently and manage multiple tasks effectively.
Apolis 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.
