About this role
About the Role ICON is seeking a Senior Clinical Research Associate to work in a large-scale, fast-paced clinical operations environment. You will collaborate with a team of qualified CRAs to identify, select, initiate and close-out investigational sites for phase II–IV studies, ensuring compliance with ICH-GCP and applicable regulations. What You'll Do
- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
- Submit protocol, consent documents for ethics/IRB approval, and prepare regulatory submissions
- Balance sponsor-generated queries and maintain study-related communications
- Take responsibility for study cost efficiency and resource utilization
- Prepare and review study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs What We're Looking For
- 18 months+ of monitoring experience in phase I-III trials as a CRA
- College degree in medicine, science, or equivalent
- Previous monitoring experience in medium-sized studies, including study start-up and close-out
- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
- Excellent written and verbal communication
- Ability to work to tight deadlines
- Availability to travel at least 60% of the time (international and domestic) and should possess a valid driving license Compensation & Benefits ICON offers competitive salary packages, annual bonuses aligned to performance, and a broad range of benefits including health insurance, retirement planning, and life assurance. ICON is an equal opportunity employer committed to inclusion, with programs such as LifeWorks and a global Employee Assistance Programme to support you and your family.