Staff Research Associate/Study Coordinator 2 - Cardiology

General Information

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Work Location: Los Angeles, USA

Onsite or Remote

Fully On-Site

Work Schedule

Monday - Friday, 8:00am- 5:00pm

Posted Date

04/19/2024

Salary Range: $28.04 - 45.11 Hourly

Employment Type

2 - Staff: Career

Duration

Indefinite

Job #

8438

Primary Duties and Responsibilities

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Play a key role with a world-renowned leader in medical research. Help advance medical knowledge and leading-edge patient care. Take your career to a higher level. You can do all this and more at UCLA Health.

Under the guidance of the Principal Investigator, you'll be responsible for a wide variety of image post-processing and measurement activities. You will facilitate the seamless acquisition of laboratory animals and vital experiment supplies while meticulously organizing image measurements within a structured database. You will develop summary tables and enter data into a dynamic database to provide the research team with a vital layer of precision for their critical work. This role offers the opportunity for exceptional growth and development as you collaborate with world-class research professionals.

Salary: $28.04 - $45.11/hour

Job Qualifications

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We're seeking a self-motivated, independent professional with:

• Knowledge of health services or clinical research methodology and principles

• Computer proficiency with Microsoft Word/Excel/Publisher/Access

• In-depth understanding of Human Subject Protection and informed consent

• Experience following strict research imaging protocols and data entry

• Outstanding communication skills

• Experience working with a diverse research population

• Knowledge or experience in working with large animals

• California phlebotomy certification, ACRP or SoCRA highly desirable

• Bachelor's or Master's degree or related research or analytical experience preferred

• Knowledge of basic statistical tests and procedures preferred

• Background in data management of clinical research protocols preferred

• Prior IRB experience and coordination of clinical studies desired

• RN licensure a plus