Drug Regulatory Affairs

Long Island University Brooklyn

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Course Info

Summary

With pressure to contain the cost and time it takes to create new products and bring them to market, professionals with expertise in regulatory affairs are highly sought after by pharmaceutical companies and medical device manufacturers, as well as by hospitals, health maintenance organizations (HMOs) and a range of other health care oriented organizations as well. The expertise of a DRA professional may be used in areas such as clinical trials, manufacturing, compliance, patenting, sales and marketing, IT, finance and scientific writing.

Career Outcomes

One can enter as a clinical research coordinator or Drug Safety Associate at their entry-level. In their mid-level, they can enter as a Clinical Research Associate or Investigator. And at the senior level, they can be appointed as a Data Manager, Director of Regulatory Affairs

About Course

Course Credential

Masters

Application Deadline

Fall 1 June, Spring 15 November

Course Availibility

Course specific Intake

Academics, GPA

English requirements

IELTS: IELTS 6.5 TOFEL: PTE: PTE 59

Course Duration

2 Years

Tuition Fees

USD$ 24000.00

*Price shown is for indicative purpose, please check with institution

IMP Notes

Location

Brooklyn, New York.

Scholarships

Here are some scholarship that are available at The Long Island University Brooklyn.

Combined Adrienne Marshall English Scholarship and Barry Marshall Science Scholarship

Value of scholarship

Tuition Fee Scholarship

Application details:

For further details, please contact the university website.

Eligibility requirements

Be students at the Beijing Huija Private School;
meet all entry requirements normally applied to the English Language Bridging course and the Bachelor of Science1 course;
not be Australian citizens or permanent residents of Australia; and
be liable for international full fees.

Who can apply:

All international