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Company Name:
Approximate Salary:
Not Specified
Location:
ROCKVILLE, Maryland
Country:
United States
Industry:
Research & Development
Position type:
Full Time
Experience level:
Education level:

Clinical Project Manager I (NCI)

Description:

PROGRAM DESCRIPTION

DCTD - ADRD/DCTD, in support of NCI/DCTD, facilitates paths of unique molecules, diagnostic tests, and therapeutic interventions to clinical applications, including distinct molecular signatures for cancer, refined molecular assays, and state-of-the-art imaging techniques that are too high-risk for industry or academia to pursue 

KEY ROLES/RESPONSIBILITIES-THIS POSITION IS CONTINGENT UPON FUNDING APPROVAL

Clinical Project Manager I

  • The new NCI The Cancer ImJaging Archive (TCIA) operational organization defines a new position of Submissions Manager.
  • This person requires knowledge of DICOM, as well as the ability to program in appropriate scripting languages, interact professionally with data submitters and solve problems arising in the data submission and curation processes
  • The additional Submissions Manager will become part of a TCIA submission curation team located in Washington DC.  Initially this team will help clear the existing backlog of collections but is intended to directly support the Apollo program
  • Adding this additional support will facilitate improvement of all phases of the TCIA workflow


Qualifications:

BASIC QUALIFICATIONS

To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below:

  • Possession of a Bachelor's degree from an accredited college/university according to the Council for Higher Education Accreditation (CHEA) in a health related field. (Additional qualifying experience may be substituted for the required education). Foreign degrees must be evaluated for U.S. equivalency.
  • In addition to the educational requirements, a minimum of six (6) years of experience related to  clinical trials
  • Familiarity of technical data requirements of radiological images, pathology images or other scientific specimens
  • Must be able to obtain and maintain a security clearance

PREFERRED QUALIFICATIONS

Candidates with these desired skills will be given preferential consideration:

  • Experience de-identifying patient data
  • Knowledge of and understanding of HIPAA requirements
  • PMP certification

Expected Competencies:

  • Solid time management and organizational skills
  • Excellent oral and written communication skills
  • Willingness to work in strict compliance with procedures, rules and regulations of the project
  • Ability to work in a team environment to define problems and find corrective actions


Leidos Overview:
Leidos is a global science and technology solutions leader working to solve the world's toughest challenges in the defense, intelligence, homeland security, civil, and health markets. The company's 33,000 employees support vital missions for government and commercial customers. Headquartered in Reston, Virginia, Leidos reported pro forma annual revenues of approximately $10 billion for the fiscal year ended January 1, 2016 after giving effect to the recently completed combination of Leidos with Lockheed Martin's Information Systems & Global Solutions business (IS&GS). For more information, visit www.Leidos.com. The company's diverse employees support vital missions for government and commercial customers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. Leidos will consider qualified applicants with criminal histories for employment in accordance with relevant Laws. Leidos is an equal opportunity employer/disability/vet.

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