Job Summary
The role of the Senior Clinical Research Associate is focused on supporting Phase I Oncology studies within a sponsor-dedicated framework in California. This position entails supervising clinical trial operations at various locations, ensuring compliance with protocols, regulatory standards, and maintaining the integrity of data while also providing mentorship.
Responsibilities
- Oversee and manage clinical trial activities across multiple sites.
- Ensure compliance with clinical trial protocols and regulatory requirements.
- Maintain the integrity of data collected during trials.
- Provide guidance and mentorship to junior staff and team members.
Qualifications
- Proven experience in clinical research, particularly in oncology.
- Strong understanding of regulatory requirements and clinical trial conduct.
- Ability to work collaboratively with various stakeholders.
- Excellent organizational and communication skills.
ICON 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.
