By Giovanna Guerr… on
Forums
Otros Trabajos STEM
Deadline

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.
Categorías de Contenido
Ciencias biológicas y de la salud