Full-Time

Data Coordinator 2

Yale University

Yale University

Compensation Overview

$31.83/hr

New Haven, CT, USA

Hybrid

Hybrid work model.

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Epic (EHR)
Inventory Management
Ruby
Word/Pages/Docs
Oracle
HIPAA
Data Analysis
Excel/Numbers/Sheets
Requirements
  • Intermediate to advanced computer proficiency with Excel and Word, with the ability to utilize electronic medical databases.
  • Ability to coordinate patient or study participant care from recruitment through off-treatment and follow-up phases, including scheduling and verifying appointments.
  • Ability to independently and accurately abstract, create, and maintain study participant research records, ensuring required data is collected, source verified, and entered into sponsor databases.
  • Ability to work with study sponsor personnel, maintain confidentiality, multitask, manage shifting priorities, and remain organized and meticulous with details.
  • Two years of related work experience in the same job family and a Bachelor's degree in a related field, or an equivalent combination of experience and education.
  • Ability to meet healthcare worker health requirements, including required vaccinations, immunity documentation, tuberculosis screening, and annual influenza vaccination.
Responsibilities
  • Research and collect data through site or home visit intakes, library research, structured interviews, or other means for research projects.
  • Interpret, synthesize, and analyze data using scientific or statistical techniques; modify and plan research experiments, procedures, tests, or survey instruments; and assist in research design.
  • Write and edit material for publication and presentation and report on the status of research activities.
  • Oversee and instruct research and support staff on technical procedures, equipment operation, and laboratory maintenance.
  • Schedule and coordinate research activities and identify and recruit study participants.
  • Order and maintain inventory of supplies.
  • Assist in preparing financial information and monitoring budgets.
  • Perform additional functions incidental to research activities.
Desired Qualifications
  • Experience coordinating, planning, or working in a high-volume, multitask setting.
  • Knowledge of Oracle software, Medidata Rave, EPIC, and ONCORE.
  • Knowledge of federal regulations for HIPAA and IRB.
  • Experience working in a clinical trials setting.
  • Oncology experience.
  • Completion of Good Clinical Practice training.

Company Size

N/A

Company Stage

N/A

Total Funding

N/A

Headquarters

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Founded

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