Unfortunately, this job posting is expired.
Don't worry, we can still help! Below, please find related information to help you with your job search.
Don't worry, we can still help! Below, please find related information to help you with your job search.
Related keywords
Some similar recruitments
Traffic Engineer Jobs
Recruited by OWN, Inc. 9 months ago
Address , Carthage, 64836
Social Studies Item Writer
Recruited by Pearson 9 months ago
Address , Pierre, 57501, Sd
6Th Grade Social Studies Teacher
Recruited by The South Bend Clinic 9 months ago
Address South Bend, IN, United States
Clinical Dvlp & Infection Prev Coordinator
Recruited by Ohana Pacific Health 10 months ago
Address Koloa, HI, United States
Social Studies Teacher Jobs
Recruited by The South Bend Clinic 10 months ago
Address South Bend, IN, United States
Traffic Engineer Jobs
Recruited by Advanced Transportation Solutions 11 months ago
Address , Rockville, 20850, Md
Research Assistant/Project Coordinator - Ed Studies - Remote
Recruited by WESTAT 1 year ago
Address , Rockville, 20850, Md
$45,000 - $60,000 a year
Social Studies Teacher (Middle Grades)
Recruited by Perquimans County Schools 1 year ago
Address , Winfall, 27985, Nc
Clinical Studies Coordinator Jobs
Company | Elevance Health |
Address | Greater Indianapolis, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-08-29 |
Posted at | 9 months ago |
- Job Family: Biostatistics and Research
- Date Posted:Jul 28, 2023
- Req #: JR78662
- Type: Full time
- MO, ST LOUIS
- GA, ATLANTA
- Florida, Miami
- TN, NASHVILLE
- OH, MASON
- IN, INDIANAPOLIS
- VA, RICHMOND
- TX, HOUSTON
- IL, CHICAGO
- Provides on-site guidance for site research staff.
- Monitors and reports adverse events.
- Identifies and recruits eligible patients from pharmacy's patient base for enrollment.
- Provides study operation insight.
- Assists in the development of study documents, case report forms, site staff training and procedure manuals.
- Assesses protocol, standard operating procedures, IRB, HIPAA and state and federal regulations compliance.
- Performs informed consent discussions with patients.
- Reviews study progress and communicates study updates to the research team.
- Requires an AAS/AS degree and a minimum of 2 years of clinical experience including site monitoring or minimum of 2 years of site coordination experience on multiple clinical studies or protocols; or any combination of education and experience which would provide an equivalent background.
- Demonstrated understanding of medical terminology, medical records and clinical trial activities strongly preferred.
- Experience with clinical studies strongly preferred.
- Intermediate proficiency with MS Excel preferred.
- Working knowledge of Immunoglobulin products and home infusion experience strongly preferred.
- Experience with medical terminology strongly preferred.
- Working knowledge of FDA regulation as a result of clinical research experience strongly preferred.
- Privacy Notice for California Residents
- EEO Policy Statement
- Pay Transparency
- Know Your Rights
-
Systems Analyst - Excel, Xml, Sql, Scripting
By CyberCoders At Salt Lake City, UT, United States 8 months ago
-
(Senior) Finance & Shared Services Manager
By Catholics For Choice At Washington, DC, United States 8 months ago
-
Paralegal - Probate Administration
By CyberCoders At Miami, FL, United States 8 months ago
-
Account Executive - Automotive Software
By ECW Search At United States 8 months ago
-
Construction Project Coordinator Jobs
By CyberCoders At River Falls, WI, United States 8 months ago