Staff Research Associate

University of California, Los Angeles, United States

Updated: almost 3 years ago
Location: Los Angeles, CALIFORNIA
Deadline: The position may have been removed or expired!

Qualifications

REQUIRED:

Experience in the preparation of research regulatory documents, informed consents, and IRB submissions.

Experience in patient-related policies and procedures in university-wide, state, and federal regulatory management of clinical trials.

Experience in data management of clinical research protocols.

Effective oral and written communications skill necessary to make inquiries and convey information.

Excellent writing skills to prepare correspondence and proofread for correct spelling, punctuation and grammar.

Organizational skills necessary to make complex arrangements.

Skill in using personal computers, working knowledge of word processing, spreadsheet, database and presentation programs.

Ability to handle confidential material with judgment and discretion

PREFERRED:

Minimum degree of BA in Biology


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