国际学生入学条件
To be eligible for admission to an associate degree program at HCC, applicants must submit documentation that they have the equivalent of one of the following:
high school equivalency certificate (GED)
Associate or higher degree
standard high school diploma
High School
If you graduated from a high school in the United States, please request that final, official transcripts be sent to HCC in a sealed envelope or electronically directly from your high school by the given application deadline. Transcripts must include your final grades and graduation date. Opened transcripts are considered to be unofficial and will not be accepted.
IELTS academic overall band score of 5.5 or higher
TOEFL score of 61 (iBT) or higher.
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雅思考试总分
5.5
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雅思考试指南
- 雅思总分:5.5
- 托福网考总分:61
- 托福笔试总分:160
- 其他语言考试:Pearson PTE academic minimum score of 46 or higher
CRICOS代码:
申请截止日期: 请与IDP顾问联系以获取详细信息。
课程简介
临床研究专业的AS学位为您准备了监视临床试验的重要角色。随着医疗保健服务的许多进步,对训练有素的医疗保健专业人员的需求与日俱增,尤其是在临床研究方面。这项新的HCC计划建立了以下基本技能:遵守IRB准则,临床研究参与者的安全性,临床治疗和研究访问的协调,研究参与者的筛选,募集和招募以及符合联邦和州法规的临床试验。临床研究专业培训使您有资格从事生物学,药学或社会和行为临床研究环境。课程包括对药物开发,联邦法规,良好的临床实践以及临床研究过程的深入研究。受监督的现场工作提供以下方面的技能应用:方案设计,参与者
The clinical research professional AS degree prepares you for the important role of monitoring clinical trials. With the many advances in healthcare delivery, there's a growing need for trained healthcare professionals, especially in clinical research. This new HCC program builds fundamental skills in adherence to IRB guidelines, safety for clinical research participants, coordination of clinical treatment and study visits, screening, recruitment, and enrollment of study participants, and clinical trial compliance with Federal and State regulatory laws. Clinical research professional training qualifies you to work in biological, pharmaceutical, or social and behavioral clinical research settings. Coursework includes an in-depth study of drug development, federal regulations, good clinical practices, and the clinical research process. Supervised fieldwork provides skills application in protocol design, participant recruitment, regulatory compliance, accountability for drugs and devices, and auditing documentation in clinical research studies.
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