Job Summary
The Clinical Research Associate at ICON Strategic Solutions plays a pivotal role within a sponsor-dedicated model where expertise is complemented by ICON’s global resources. This position demands a thorough understanding of clinical trials and research processes in a multi-therapeutic area context.
Responsibilities
- Collaborate directly with sponsors to ensure successful execution of clinical trials.
- Oversee the recruitment and management of study sites.
- Conduct site visits and audits to monitor compliance with study protocols.
- Manage data collection and documentation to maintain the integrity of study results.
- Facilitate communication between the study team and stakeholders.
Qualifications
- Bachelor’s degree in a relevant discipline, such as life sciences, nursing, or medicine.
- Considerable experience in clinical research, preferably as a Clinical Research Associate.
- Strong organizational skills and attention to detail.
- Ability to work effectively in a team-oriented environment.
- Excellent communication skills, both verbal and written.
ICON Clinical Research 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.
