clinical research professional i - Little Rock, AR, United States - Arkansas Children's Hospital

Arkansas Children's Hospital Little Rock, AR, United States

3 weeks ago

Description

ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OPPORTUNITY EMPLOYER.

ALL QUALIFIED APPLICANTS WILL RECEIVE CONSIDERATION FOR EMPLOYMENT WITHOUT REGARD TO RACE, COLOR, RELIGION, SEX, SEXUAL ORIENTATION, GENDER IDENTITY OR EXPRESSION, NATIONAL ORIGIN, AGE, DISABILITY, PROTECTED VETERAN STATUS OR ANY OTHER CHARACTERISTIC PROTECTED BY FEDERAL, STATE, OR LOCAL LAWS.

CURRENT EMPLOYEES:
Please apply via the internal career site by logging into your Workday Account )and search the Find Jobs report.

Work Shift:
Please see job description for details.

Time Type:
Full time

Department:
CC033020 Clinical Research Operations

Summary:
The Clinical Research Professional I coordinates selected specific aspects of clinical research studies.

This role serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study.

Additional Information:

Required Education:

Bachelor's degree from four-year college or university; Or four years related experience and/or training; or equivalent combination of education and experience.

Recommended Education:

Required Work Experience:

Recommended Work Experience:
Related Field - 1 year of experience

Required Certifications:

Recommended Certifications:
Certified Clinical Reseach Coordinator (CCRC) - Academy of Clinical Research Professionals, Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates

Description

Recruits and screens patients for enrollment eligibility and participation in research projects. Obtains consent for participation in accordance with all government regulations and internal policies/procedures.
Prepares flowcharts, study specific source documents, and collects/records subject data on case report forms. Creates databases and performs date entry into the database.
Serves as a research resource to subjects, families, and other healthcare providers regarding the needs of study and subjects family preserving patient/subject privacy and maintaining confidentiality of subject information.
Promotes knowledge of current professional practice and research standards, laws and regulations that affect human subjects research.
Facilitates and improves collaboration with other departments to facilitate research across the continuum.
Coordinates/collects requested data for sponsor review during site visits. Assists study monitor(s) in chart and case report form review.
Maintains files and study documentation according to institutional and regulatory standards
Performs other duties as assigned.

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