Job Summary
The role of Senior Clinical Research Associate involves providing essential support for oncology clinical trials within a sponsor-dedicated framework, specifically focusing on the South Central region. The position requires engagement in site management and monitoring—both remotely and in-person—ensuring the integrity of data and adherence to regulatory standards for solid tumor studies.
Responsibilities
- Oversee site management and ensure proper execution of clinical trials.
- Conduct both remote and onsite monitoring to ensure compliance with study protocols.
- Maintain oversight of data integrity throughout the trial process.
- Ensure adherence to all regulatory requirements related to clinical trials.
Qualifications
- Experience in oncology clinical trials and solid tumor studies.
- Strong knowledge of regulatory compliance and clinical research standards.
- Proficient in site management and monitoring techniques.
- Excellent communication and organizational 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.
