
Clinical Research Associate Role
1 week ago
Clinical research associates are key professionals in the design, analysis, and interpretation of clinical trials. We seek experienced CRA II/Senior CRA to join our team.
Responsibilities:- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 4 years of experience as a Clinical Research Associate.
- Deep 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.
- Varying annual leave entitlements.
- A range of health insurance options.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour support access.
- Life assurance.
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
We prioritize diversity and inclusion. Our culture values innovation, excellence, and employee growth. We strive to provide a workplace free from discrimination and harassment.
For qualified candidates, we offer equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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