Clinical Research Associate: Thrive in a Dynamic Environment
hace 1 mes
At ICON Plc, we're on a mission to shape the future of clinical development. As a Clinical Research Associate, you'll play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Job Description:We are seeking a skilled Clinical Research Associate to join our diverse and dynamic team. In this role, you will:
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials with meticulous attention to detail.
- 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.
To succeed in this role, you should have:
- A Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- 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.
We offer a competitive salary range of $60,000 - $80,000 per year, depending on location and experience. Our benefits package includes:
- Variety of annual leave entitlements.
- A range of health insurance offerings to suit your needs.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme.
- LIFE assurance.
- Flexible country-specific optional benefits.
At ICON Plc, we value diversity and inclusion. We are committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive 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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