Job Description:

Description

The Clinical Research Coordinator (CRC) is responsible for coordinating and collaborating with principle investigators on multiple ongoing research studies in an effort to facilitate research at CHRISTUS St. Vincent Health System. This position will market CHRISTUS research services, create and maintain research activity databases, and monitor the impacts of the research studies to include financial and safety risks. While the Principal Investigator is ultimately responsible for the clinical trial, the CRC is responsible for the facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The CRC works collaboratively with the entire CSV team, sponsors, and monitors to ensure productivity and timely completion of studies.

Requirements

EDUCATION: High School Diploma or equivalent required. Bachelor's Degree in Healthcare Administration, Research, Business or related field preferred.

CERTIFICATION/LICENSES: N/A

SKILLS:

- Proficiency in using computer databases, spreadsheets and word processing software, and electronic health systems used in research environment, or have a willingness to learn and demonstrate proficiency within six months of hire

- Requires excellent oral and written communication skills

- Requires excellent organizational skills and knowledge of federal legislation regarding human subject research and the provision of health care is also required

- Expertise in applying for research protocols is required

- Proficient in organizing and examining data

- Must be able to produce clear and concise products

- Must be thorough in gathering and reporting information

- Must be flexible and be able to relate well with a variety of people.

EXPERIENCE: Three years of experience healthcare.

NATURE OF SUPERVISION:

-Responsible to: Regional Research Director

ENVIRONMENT:

- Bloodborne pathogen B

General office environment, frequent contact with patients, VDT exposure.

PHYSICAL REQUIREMENTS: Long periods of sitting at times. Keyboard usage with sound ergonomic principles. Must be flexible in work schedule and willing to travel between research sites

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