Job Title:Product Development Project Manager - NIAID - MP
Department:Department Of Health And Human Services
Agency:National Institutes of Health
Job Announcement Number:NIH-NIAID-MP-13-862032
This position is closed and no longer accepting online applications through USAJOBS.
The contents of the announcement can still be viewed.
/ Per Year|
|Friday, March 22, 2013 to
Tuesday, March 26, 2013|
SERIES & GRADE:
|Full Time -
Agency Employees Only|
|1 vacancy in the following location:|
Montgomery County, MD United StatesView Map
WHO MAY APPLY:
|Current Permanent Title 5 NIH employees and individuals under CTAP only.|
The position is located within the Bacteriology & Mycology Branch (BMB), Division of Microbiology and Infectious Diseases (DMID), National Institute of Allergy and Infectious Diseases.
The DMID supports extramural research related to the control and prevention of diseases caused by virtually all human infectious agents except HIV. The BMB directly manages a portfolio of grants and contracts awarded to outside institutions for research on fungal diseases and select bacterial pathogens. It also includes all areas of basic, applied, and clinical research for all of the invasive mycoses. The position is critical to DMID's domestic and international efforts to develop vaccines for potential bioterrorism agents (e.g. smallpox, anthrax, plague, and botulism).
- Time in grade met within 30 days of closing date.
- Position is subject to a background investigation.
- This position requires overnight travel that might be 1 night per month.
DUTIES:Back to top
If selected for this position you will perform the following duties:
Serve as project manager for DMIDs project development contracts and grants.
Mediate and coordinate the activities of product development teams to assure productive and timely work on specific product development projects.
Develop Requests for Proposals and other documents required for solicitation and review of proposals.
Prepare detailed site visit and analysis reports and written reviews, batch records and other cGMP (Good Manufacturing Practices) associated documentation.
Serve as Branch liaison with the Office of Regulatory Affairs, Office of Clinical Research Affairs on all cGMP compliance-related activities and issues.
Represent the Division and the Institute in the interpretation and application of regulations, policies, procedures and practices related to product development and related activities.
QUALIFICATIONS REQUIRED:Back to top
You must possess a full 4-year course of study in an accredited college or university leading to a bachelor's or higher degree with major study in an academic field related to the health sciences or allied sciences appropriate to the work of the position.
In addition to the basic education requirements:
You must demonstrate in your resume at least one (1) year of specialized experience equivalent to at least the GS-12 level in the Federal service obtained in either the private or public sector performing the following types of tasks: resolving complex problems relevant to product development activities; coordinating project efforts for a research or product development team; managing scientific projects using computer-based programs; performing research using methodologies related to infectious diseases.
View Assessment Questions
This position has an education requirement. You must submit a copy of your transcripts (or a list of your courses including titles, credit hours completed and grades). Unofficial transcripts will be accepted in the application package; however, official transcripts will be required prior to receiving an official offer. Click here for information on Foreign Education . If you are currently or were previously in this occupation series you do not need to submit transcripts. Instead, submit an SF-50 showing the appointment in this occupational series.
Males born after December 31, 1959 must be registered with Selective Service.
HOW YOU WILL BE EVALUATED: