2 Job Opportunities at NCCAM
Submitted by Giovanna Guerrero-Medina on
Forums:
Deadline:
Friday, 16 August 2013
https://www.usajobs.gov/GetJob/ViewDetails/349405300
SALARY RANGE: |
$89,033.00 to $115,742.00 / Per Year |
OPEN PERIOD: |
Monday, August 12, 2013 to Saturday, August 17, 2013 |
SERIES & GRADE: |
GS-0601-13 |
POSITION INFORMATION: |
Full Time - Permanent |
PROMOTION POTENTIAL: 13 |
|
DUTY LOCATIONS: |
1 vacancy in the following location: Montgomery County, MD United StatesView Map |
WHO MAY APPLY: |
United States Citizens |
DUTIES:
- Reviews and tracks data collected on the NCCAM clinical research portfolio.
- Plans, develops, and implements oversight of targeted research programs.
- Reviews and manages patient safety data, implementing necessary changes in study conduct based on safety data.
- Directs development and maintenance of standard operating procedures for adverse event data collection, processing and reporting systems.
- Performs oversight/management pertaining to the regulatory and procedural aspects of clinical site monitoring and performance evaluation.
- Oversees tracking of Investigational New Drug (IND), Investigational Device Exemption (IDE) and Pre-Marketing Application (PMA), progress reports, and other related paperwork.
https://www.usajobs.gov/GetJob/ViewDetails/349210300
SALARY RANGE: |
$89,033.00 to $115,742.00 / Per Year |
OPEN PERIOD: |
Monday, August 12, 2013 to Friday, August 16, 2013 |
SERIES & GRADE: |
GS-0601-13 |
POSITION INFORMATION: |
Full Time - Permanent |
PROMOTION POTENTIAL: 13 |
|
DUTY LOCATIONS: |
1 vacancy in the following location: Montgomery County, MD United StatesView Map |
WHO MAY APPLY: |
This vacancy is open to current permanent Title 5 employees and individuals eligible under CTAP only. Title 42 employees are not eligible. |
DUTIES:
- Reviews and tracks data collected on the NCCAM clinical research portfolio.
- Plans, develops, and implements oversight of targeted research programs.
- Reviews and manages patient safety data, implementing necessary changes in study conduct based on safety data.
- Directs development and maintenance of standard operating procedures for adverse event data collection, processing and reporting systems.
- Performs oversight/management pertaining to the regulatory and procedural aspects of clinical site monitoring and performance evaluation.
- Oversees tracking of Investigational New Drug (IND), Investigational Device Exemption (IDE) and Pre-Marketing Application (PMA), progress reports, and other related paperwork.
