Job Summary
The position of Senior Clinical Research Associate in Early Clinical Development at IQVIA Biotech based in San Francisco, California, focuses on supervising clinical trial sites. The role is essential for ensuring compliance with study protocols, regulatory standards, and effective management of data queries.
Responsibilities
- Oversee monitoring activities at clinical trial sites to confirm adherence to protocols and regulations.
- Resolve data queries effectively to ensure the integrity of clinical trial data.
- Maintain comprehensive Trial Master Files and Investigator Site Files, including all critical regulatory documents.
Qualifications
- Proven experience in clinical research monitoring and compliance verification.
- Strong understanding of regulatory requirements related to clinical trials.
- Ability to communicate effectively with clinical teams and stakeholders.
IQVIA 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.
