Job Summary
The Senior Clinical Research Associate role at ICON is focused on managing Phase I clinical trial operations in Oncology throughout various locations on the West Coast of California. This position is vital for ensuring that clinical trials meet regulatory standards while achieving their intended outcomes.
Responsibilities
- Oversee and monitor the activities associated with Phase I Oncology clinical trials.
- Ensure compliance with protocol and regulatory requirements during the trial process.
- Lead and coordinate the efforts of the clinical research team.
- Conduct site visits to assess trial progress and address any issues that may arise.
- Interact with site staff to provide guidance and maintain study quality.
Qualifications
- Extensive experience in clinical research, particularly in Oncology.
- Strong understanding of regulatory guidelines and compliance standards.
- Excellent leadership and communication skills.
- Ability to work effectively with cross-functional teams.
- A proactive approach to problem-solving and trial management.
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.
