学历文凭
Associate Degree
专业院系
临床检验学
开学时间
课程时长
课程学费
国际学生入学条件
high school equivalency certificate (GED)
Associate or higher degree
standard high school diploma
If you graduated from a high school outside of the United States, your transcripts, graduation certificates and/or exam results must be evaluated by a NACES-approved agency to prove equivalency with a U.S. high school diploma.
Official Transcripts from all institutions attended be sent to HCC in a sealed envelope or electronically directly from the issuing institution.
TOEFL score of 61 (iBT) or higher
IELTS Academic overall band score of 5.5 or higher
iTEP Academic score of 4.0 or higher
STEP Eiken minimum score of Grade 2A or higher
Applicants with less than a 2.0 college minimum cumulative grade point average (GPA) in a grading structure whose maximum GPA is 4.0, excluding college preparatory courses, will not be considered for admissions. This cumulative GPA includes courses from all higher education institutions attended.
IDP—雅思考试联合主办方
雅思考试总分
5.5
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- 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
课程简介
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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