Clinical Research Associate II Specialist
Vor 7 Tagen
We are seeking a highly skilled Clinical Research Associate II Specialist to join our team. As a Clinical Research Associate II Specialist, 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.
Key Responsibilities:
- 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.
- 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.
At ICON, we offer a competitive salary, a range of benefits, and opportunities for professional growth and development. Our benefits include various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program. We are an equal opportunity employer and welcome applications from diverse candidates.
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