Job details
Job type full-time
Full job description
Process advisor iv
Washington, dc
Employment type: full time
Clearance requirements: naci
Flsa status: exempt (salary)
Eligible for remote work: yes
Goldbelt frontier fosters a collaborative environment where our employees are encouraged to utilize and employ their operational and leadership skills – many of our senior project managers and business analysts are recognized as subject matter experts in their fieldsWe understand how to work with and support multiple stakeholders to aid in the development and implementation of national policies, strategies, and doctrine.
Essential job functions:
Possess expertise conducting literature review and market research.
Possess experience performing healthcare-related data analysis, data management, and problem solving.
Possess excellent written and verbal communication skills including experience with unstructured verbal interactions, briefings, and meeting moderation.
Possess demonstrated experience conceptualizing research directions, analyzing trends, and helping develop justifications for new research and development investments.
Be able to analyze, summarize, and communicate the intellectual content of scientific and technological information to both scientific and lay audiences quickly and effectively.
Possess demonstrated experience in working with, managing, and designing methods for collection of health-related information and personal health information.
Possess experience leading research and development projects and teams.
Possess demonstrated experience providing scientific advice to senior government leaders.
Possess demonstrated experience in assisting with coordinating potential research collaborations with other federal government agencies, industry, and international organizations.
Necessary skills and knowledge:
Support the technical aspects of therapeutic administration, use, and other related projects within the team, working in tandem with the overall therapeutics program lead and the therapeutics operational action officer.
Engage with stakeholders to understand technical information related to adoption of new and existing covid-19 therapeutics.
Support the technical aspects of administration and use of covid therapies.
Conduct research and maintain reliable information sources.
Maintain administrative record for all program files.
Perform data collection and analysis.
Develop and review material for leadership briefs, ea engagement, white house briefings, etc.
Serve as support for aspr and external engagements.
Assist in the development of strategic and operational plans and approaches.
Develop and execute on covid-19 therapeutic awareness strategies.
Write and edit materials, such as reports, regulations, scholarly works, reference works and speeches.
Draft articles for review for possible submission to technical journals, command information publications and other media covering significant accomplishments of aspr/cmo/io.
Obtain and clearly explain information on a variety of medical or scientific program, policy and research issues and educational materials.
Communicate scientific information effectively both orally and written (e.gBriefing presentations, technical documents, etc.).
Analyze and evaluate projects, proposals and plans, and metrics for technical and programmatic merit, as well as to identify risks, mitigation strategies and potential areas of improvements.
Identify and review emerging requirements and opportunities for transition and application of selected technologies.
Assist in leading technical discussions with government and industry regarding program concepts, funded projects, strategies and transition concepts.
Collaborate with project teams and participate in the evaluation of technical results in multiple developmental areas, developing strategies to move the program forward.
Provide periodic update reports to pms.
Maintain current knowledge on new technologies and methodologies that may benefit the program, assessing technical proposals critically and effectively, providing written technical opinion on the feasibility of new technologies, and organizing brown bag seminars to review the technologies.
Review and search scientific literature and databases in order to identify technical information and to provide references to support product development efforts.
Minimum qualifications:
Possess a doctoral degree in biological sciences, engineering, a healthcare-related field or a related discipline.
Possess at least five (5) years of relevant experience (e.g., laboratory clinician, research clinician, pharmacist, or other healthcare setting).
Preferred qualifications:
Possess experience in conducting and publishing clinical research.
