About this role
About the Role ICON is seeking CRAs II & Senior CRAs (Sponsor-Dedicated / Multisponsor) to join our diverse and dynamic team. You will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What You'll Do
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolution of queries to maintain high-quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
What We're Looking For
- Bachelor’s degree in a scientific or healthcare-related field.
- Minimum 1.5 years of monitoring experience for the CRA II role and 2 years for the Senior CRA role (Required).
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Ability to travel at least 60% of the time.
Compensation & Benefits
- Competitive salary and a range of benefits focused on well-being and work-life balance.
- Annual leave entitlements and health insurance offerings.
- Competitive retirement planning offerings to maximize savings.
- Global Employee Assistance Programme with 24-hour access to a network of professionals.
- Life assurance and flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments).
- ICON is committed to inclusion, belonging, and providing an accessible environment for all candidates.