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Benefits
Scholarship Opportunities
Apply
online
Call our Employment Center at (304) 388-7458 or (800)
323-5157
Visit us at 511 Brooks Street, Charleston, WV 25301
Office Hours: Monday through Friday - 8:00 am to 4:30 pm
Write us at Post Office Box 1547,
Charleston, WV 25326
Charleston Area Medical Center Health System is an equal opportunity employer, m/f/d/v
We are currently accepting applications for the following positions...
| Position Available | Status | Company |
| Cook | Full-time | CAMC |
| Dietary Clerk | Full-time | CAMC |
| Health Unit Coordinator | Full-time | CAMC |
| HIM Chart Prep Tech | Full-time | CAMC |
| HIM Chart Scanner | Full-time | CAMC |
| Housekeeper | Part-time | CAMC |
| Laundry Technician | Full-time | CAMC |
| Medical Records Clerk | select one | CAMC |
In addition to the above Support Services positions we have the following...
| Position Available | Status | Company | Description |
| Collector I | Full-time | CAMC | Effective collection of problem and delinquent accounts. Requires a High School diploma or GED with 1 year of telecommunications or account collection experience and 40 wpm. |
| Dental Assistant | Full-time | Integrated | Experienced dental assistant and new graduate opportunities available. |
| Medical Assistant- Certified | Full-time | Integrated | Provide optimum assistance to the health care provider and patient. Perform patient registration, discharge, and other related services for the area assigned. |
| Research Assistant | Full-time | CHERI | Basic Function To provide support to Principal Investigator and Study Coordinator in all appropriate functions related to the conduct of a research investigation. Duties and Responsibilities Essential Duties: 1. Process and organize new protocol as it arrives. 2. Process IRB and IACUC packets for signatures and approvals as directed. 3. Maintain accurate filing for protocols for tracking original and subsequent activity on protocols and approval documentation. 4. Process addendums to active protocols. 5. Assist Coordinator in preparing documents for institutional grants and research office and for IRB. 6. Assist in the preparation of grant applications and editing of articles and manuscripts. 7. Search scientific journals for information. 8. Communicate the data gathered from research activities to Principal Investigator. 9. Document that IRB has been notified of a protocol change that is administrative or significant; confirm all IRB approvals. 10. Assist Clinical Trial Coordinator in performing telephone and written communications with physician providers and patients. 11. Excellent writing skills. 12. Collect and manage data needed per study. Qualifications for the Position Minimum Required Level of Education/Training BACHELOR RELATED Minimum Required Experience 1 YEAR RELATED EXPERIENCE OTHER YEARS experience &/or interest in maintaining the animal lab- preferred FAMILIARITY OF BASIC PC SKILLS YES TYPE OF SOFTWARE word processing and data managementsoftware May Substitute Associate degree in related field of research dep. on for Bachelors degree and 1 yr related exp. Comments Ability to obtain and interpret information and apply protocol/data to patients as directed by the Principal Investigator or Study Coordinator. |