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SharePoint Administrator III

Summary Sheet: Administration

Advertiser NameFrederick National Laboratory for Cancer ResearchAdvertiser Type:Agency
Country:United StatesLocation:United States
Language:English - United Kingdom (en-GB) Contact Name:
Employment Type:PermanentWorkhours:Full Time

Position: SharePoint Administrator III


SharePoint Administrator III

Job ID: req3364
Employee Type: exempt full-time
Division: Clinical Monitoring Research Program
Facility: Rockville: Fishers Ln
Location: 5601 Fishers Ln, Rockville, MD 20852 USA

The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.

Accountability, Compassion, Collaboration, Dedication, Integrity and Versatility; it's the FNL way.


Within Leidos Biomedical Research Inc., operator of the Frederick National Laboratory for Cancer Research, the Clinical Monitoring Research Program Directorate (CMRPD) provides high-quality comprehensive and strategic operational support to high-profile domestic and international clinical research initiatives sponsored by the National Cancer Institute (NCI), the National Institute of Allergy and Infectious Diseases (NIAID), the National Institutes of Health (NIH), and several other institutes within NIH. CMRPD's ability to provide rapid responses and high-quality solutions, and to recruit and retain experts with a variety of backgrounds, allows the directorate to facilitate strategic support to the growing clinical research portfolios of NCI, NIAID, and other NIH divisions/offices/centers. CMRPD's support services are aligned with the program's mission to provide comprehensive clinical trials operations and program/project management services to advance scientific clinical research that complies with applicable regulations and guidelines, maintains data integrity, and protects human subjects. CMRPD services include clinical trials monitoring, regulatory affairs support, clinical safety oversight, protocol navigation/protocol development, and programmatic and project management support to facilitate the conduct of more than 400 Phase I, II, and III domestic and international trials annually. These trials investigate the prevention, diagnosis and treatment of cancer, influenza, HIV, infectious diseases and emerging health challenges like Ebola virus and COVID-19, heart, lung, and blood disorders, parasitic infections, and rare and neglected diseases. CMRPD's collaborative approach to clinical research support and the expertise and dedication of staff to the continuation and success of CMRPD's mission has contributed to improving the overall standards of public health on a global scale.

The Clinical Monitoring Research Program Directorate (CMRPD) provides collaborative leadership and management oversight and coordination of special research projects for the NIAID, Division of Clinical Research (DCR), Office of Planning and Operations Support (OPOS).


  • Identifies technology business needs, analyzes current enterprise solutions, and aligns these data with a shared / integrated business model

  • Provides consistency to the alignment of the technical perspective but also with the logical user interaction based on shared business concepts

  • Assists in turning the identified technology business needs into deliverables and helps in the overall planning, monitoring, and execution of a work plan

  • Assists in the staging and planning of project phases, monitoring milestones, and the continued tailoring of work product to the mission and operational logic

  • Provides status management for incoming issues or requests, general solution strategy, and providing input to the team for overall technology governance

  • Develops and manages folder structures, document curation, and facilitates account management for user access and permissions to collaborative platforms such as SharePoint, Huddle, LabKey, or others

  • Provides user training on collaborative platforms such as Huddle, SharePoint, LabKey, or others

  • This position is located at Fishers Lane, Rockville, Maryland with possibility of full time telework


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 related field. (Additional qualifying experience may be substituted for the required education)

  • Foreign degrees must be evaluated for U.S. equivalency

  • In addition to education requirements, a minimum of five (5) years related experience in developing, constructing, administering, and managing Microsoft SharePoint site collections

  • Experience in software development lifecycle of information systems

  • Ability to gather and interpret business requirements

  • Ability to communicate software demonstrations to technical and non-technical colleagues

  • Working knowledge of process and workflow design and documentation

  • Working knowledge of database technologies, including relational (SQL) and non-relational (NoSQL) databases

  • Ability to communicate effectively, orally and in writing, with non-technical and technical staff, from internal department, senior management, and the customer regarding contractual, operational, and policy related matters

  • Detail-oriented and possess strong organizational and analytical skills, with the ability to prioritize multiple tasks/projects

  • Broad range of knowledge of information systems, technical infrastructure, and ability to fulfill project requirements innovatively and independently

  • Possess knowledge of appropriate government regulations and program management

  • Ability to obtain and maintain a security clearance


Candidates with these desired skills will be given preferential consideration:

  • Experience working with clinical research data and systems such as LabKey

  • Knowledge of or familiarity with scientific data, instrumentation, and data standards including networking and cybersecurity considerations

  • Experience working with and meeting the needs of researchers, statisticians, and/or data scientists

Equal Opportunity Employer (EOE) Minority/Female/Disabled/Veteran (M/F/D/V) Drug Free Workplace (DFW)

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