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Clinical Research Associate
2 months ago
As a Clinical Research Associate at ICON, you will play a critical role in the success of our global clinical trials. We are seeking an experienced and skilled professional to join our team and contribute to the delivery of high-quality clinical research services.
Key Responsibilities- Site Selection and Management: Identify and select suitable clinical trial sites, ensuring compliance with regulatory requirements and good clinical practice (GCP) guidelines.
- Study Conduct and Monitoring: Conduct site initiation visits, routine monitoring visits, and close-out visits to ensure the integrity and quality of clinical trial data.
- Quality Assurance and Control: Oversee all aspects of study site management to ensure high-quality data, consistently low query levels, and good Quality Assurance reports.
- Education and Experience: Degree in Pharmacy or a related field, with a minimum of 2 years of prior monitoring experience in global trials within a Contract Research Organization (CRO) or pharmaceutical company.
- Skills and Knowledge: Excellent written and verbal communication skills, strong knowledge of international guidelines (ICH-GCP) and local regulations, and flexibility to travel and work from the sponsor office.
At ICON, we value our employees and offer a range of benefits to support their well-being and career development. These include:
- Competitive Salary and Benefits: A comprehensive compensation package, including annual leave entitlements, health insurance, and retirement planning options.
- Professional Development Opportunities: Training and development programs to enhance your skills and knowledge, and support your career growth within the company.
- Diverse and Inclusive Work Environment: A culture that values diversity, inclusion, and belonging, and provides opportunities for collaboration and networking with colleagues from diverse backgrounds.