Company

PricesenzSee more

addressAddressBethesda, MD
type Form of workFull-Time
CategorySales/marketing

Job description

Job Description

Location: IC: NINDS Street: 10 Center Dr Bldg: 10Room: 7D38 City: BethesdaState & Zip:MD 20814

Weekly Hours - FT: 30-40 hours per week

Overall Position Summary and Objectives

The primary role for this Research Coordinator (RC) position is to provide Clinical Research coordination and protocol navigation for the NINDS Intramural Research Program.

Min Education - Bachelor's
Resume Max Pages - 3
Certifications & Licenses -
  • Association of Clinical Research Professionals Certified Professional (ACRP-CP)

  • Association of Clinical Research Professionals (ACRP)

  • Certified Clinical Research Professional (CCRP)

  • Certified Clinical Research Coordinator (CCRC)

  • Certified Clinical Research Associate (CCRA

Field of Study -
  • Miscellaneous Health Medical Professions

  • Nursing

  • Community and Public Health

  • General Medical and Health Services

  • Neuroscience

  • Miscellaneous Biology

  • Cognitive Science and Biopsychology

  • Biology

  • Genetics

  • Health and Medical Preparatory Programs

  • Nutrition Sciences

  • Pharmacy

  • Pharmaceutical Sciences and Administration

  • Treatment Therapy Professions

  • Communication Disorders Sciences and Services

  • Sociology

  • Miscellaneous Social Sciences

  • Interdisciplinary Social Sciences

  • General Social Sciences

  • Miscellaneous Psychology

  • Clinical Psychology

  • Psychology

  • Social Psychology

  • Social Work

  • Chemistry

  • Multi-Disciplinary or General Science

Software -
  • Clinical Trial Management System (CTMS)
  • Electronic Medical Records System
  • Electronic Data Capture System
Skills -
  • Overseeing and documenting IP dispensing, inventory and reconciliation

  • Closing clinical trial sites down on completion of clinical trial

  • Ordering, tracking, and managing IP and trial materials

  • Implementation of clinical trial site action plans

  • Training clinical trial site staff

  • Coordinating project meetings

  • Previous clinical trial work

  • Electronic medical records

  • Protocol review revision Phase I or II experience

  • Patient confidentiality

  • Remote site monitoring

  • Regulatory compliance

  • Protocol development

  • Clinical Research

  • Protocol writing

  • Clinical Trials

  • Data Monitoring

  • Data Integrity

  • Patient care

  • Recruitment

  • Scheduling

  • Screening

  • Research

  • ICH/GCP

  • SOPs

  • Liaising with regulatory authorities

Statement of Work Details

Supports clinical staff develop, implement and maintain Clinical Research data files and materials.

  • Assist preparing and submitting for review accurate source documents related to all research procedures.
Refer code: 8689442. Pricesenz - The previous day - 2024-03-23 02:41

Pricesenz

Bethesda, MD
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