Job Summary
The Clinical Research Associate II position is located in Texas and offers an onsite work arrangement. This role is crucial within a global contract research organization that specializes in sponsor-centric monitoring of clinical trials. The primary focus is to ensure safety during the execution of clinical studies.
Responsibilities
- Oversee and monitor clinical trial activities to ensure compliance with protocols and regulations.
- Collaborate with investigators and site staff to enhance the efficiency of study operations.
- Ensure patient safety throughout the duration of the trial.
Qualifications
- Experience in clinical research monitoring preferred.
- Strong communication and interpersonal skills.
- Ability to work effectively in a team-oriented environment.
- Knowledge of GCP and regulatory requirements.
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.
