SME I- Clincial SME Job at Chenega Corporation

Chenega Corporation Georgia

Overview:
Come join a company that strives for Extraordinary People and Exceptional Performance! Chenega Enterprise Systems and Solutions, LLC, a Chenega Professional Services’ company, is looking for a Subject Matter Expert to support the Poxvirus and Rabies Branch (PRB) to enhance, increase and maintain the laboratory, epidemiology, and public health capacity to respond to infectious disease threats, including but not limited to MPOX disease. This position shall perform specified portions of scientific work involving MPOX case surveillance data, special investigations support, and communications/services to public health partners.

We are looking for creative, collaborative, experienced, and driven individuals to join our team! Our company offers employees the opportunity to join a team where there is a robust employee benefits program, management engagement, quality leadership, an atmosphere of teamwork, recognition for performance, and promotion opportunities. We actively strive to channel our highly engaged employee’s knowledge, critical thinking, and determination to innovate scalable solutions for our clients.
Responsibilities:
  • Identify key clinical research gaps and design studies to answer these important questions. Lead analysis and interpretation of clinical data under supervision of supervisor. Coordinate all levels of approval for project proposals (e.g., Coordination of review by Human Subjects experts). Write or supervise manuscripts about these analyses.
  • Maintain familiarity with frequently asked questions and support phone duty staff with clinical questions received from clinicians and the public.
  • Coordinate efforts to develop or update policy for use of mpox vaccines and therapeutics (e.g., recommendations of the Advisory Committee on Immunization Practices and interim recommendations for use of medical countermeasures to treat mpox). Gather input, solicit document reviews, and coordinate dissemination of policy recommendations. Create tools and informational materials for end-users of the clinical guidelines.
  • Assist with drafting text and managing reference files for manuscripts (including those not first authored by the clinical officer), collect, and collate reviewer feedback to support manuscript revisions, and facilitate manuscript submission to eClearance and MMWR.
Qualifications:
  • Master’s , PHD, MD degree in a relevant field
  • 12+ years of experience

Knowledge, Skills and Abilities:
  • Performs directed subject matter work.
  • Supports team in producing high-quality deliverable in time efficient manner.
  • Meets with client as needed.
Teleworking Permitted?: true Teleworking Details: Hybrid, must be in Georgia



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