Clinical Trials Program Specialist

National Institutes of Health · Department of Health and Human Services

Federal · USAJOBS
Lugar
Montgomery County, MD
Sueldo
$121,785 – $158,322 al año
Fechas
Publicado 2 nov · Cierra 9 nov
Ver y solicitar en USAJOBS

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Este tipo de trabajo

Empleo del gobierno federal de Estados Unidos. Se solicita en USAJOBS con un résumé federal, tiene fecha de cierre y el sueldo sigue escalas fijas (GS u otras).

El sueldo, en claro

Unos $121,785–$158,322 al año, o $58.55–$76.12 por hora a tiempo completo (40 horas). Antes de impuestos y descuentos.

Lo que piden, en corto
  • Bachillerato
Documentos que suelen pedir
  • Résumé federal (con horas por semana y fechas de cada empleo)
  • Transcripción de créditos, si el puesto pide estudios
  • Formulario DD-214 si reclamas preferencia de veterano
  • Formulario SF-50 si ya eres empleado federal
  • Identificación con foto y Seguro Social o permiso de trabajo (formulario I-9)
En nuestro catálogo

Publicada hace 4 días.

Sobre el empleo

El anuncio original está en inglés.

We are seeking a qualified individual to serve as a Clinical Trials Program Specialist, overseeing policies and procedures for NIDDK funded clinical studies. This role supports clinical research planning and management across all NIDDK divisions.

Requisitos

To qualify for a Clinical Trials Program Specialist at the GS-0601-13 level you must: Have successfully completed a full 4 year course of study in an accredited college or university leading to a bachelor's degree or graduate/higher level degree with major study in an academic field related to the medical field, health sciences or allied sciences appropriate to the work of the position. (This degree must be from an educational program from an accrediting body recognized by the U.S. Department of Education at the time the degree was obtained). AND You must demonstrate in your resume at least one (1) year of qualifying 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: Overseeing the management of large, multi-site clinical trials; Applying Federal regulations, policies, guidance, and reporting requirements governing clinical research and human subjects protections; Developing clinical research policies, procedures, standard operating procedures, tools, or funding requirements; Coordinating clinical research activities among multiple stakeholders, to include providing technical consultation; AND Conducting quality assurance and compliance activities for clinical research. You will receive credit for all experience material to the position, including experience gained in religious, civic, welfare, service, and organizational activities, regardless of whether you received pay. Do not copy and paste the duties or specialized experience from this announcement into your resume as that will not be considered a demonstration of your qualifications for this position. We may verify or assess your qualifications at any time. Inflated or unsupported qualifications may affect your rating. Any misrepresentation or material omission of facts may be sufficient cause to end further consideration of your candidacy. Persons listed as knowing your past accomplishments or experience in your application may be contacted for verification purposes at any time. Verification may, but need not, begin before receiving an offer. Preview application questionnaire before you apply: https://apply.usastaffing.gov/ViewQuestionnaire/13094350

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