Imaging Clinical Research Coordinator

Jefferson Health

Philadelphia (Philadelphia County)

On-site

USD 60,000 - 90,000

Full time

12 days ago

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Job summary

Jefferson Health is seeking staff to oversee day-to-day activities of clinical trials in accordance with Good Clinical Practice (GCP). The role involves data management, biospecimen processing, and clerical tasks to assist investigators with organizing and compiling clinical research data.

The position includes recruiting and consenting subjects, conducting study visits, and supporting regulatory submissions. Strong regulatory knowledge and ability to manage multiple tasks are required.

Qualifications

  • High School Diploma/GED or equivalent.
  • 4 years of relevant experience.
  • Knowledge of technology tools to organize, store and manage database systems.
  • Knowledge of tools for gathering and reporting data in a department.
  • Knowledge of healthcare legislation and regulatory bodies.

Responsibilities

  • Interacts with co-workers, visitors, and staff per Jefferson values.
  • Supports clinical trials with data base, biospecimen processing and clerical duties.
  • Organizes and maintains documentation for clinical trials.
  • Alerts PI on patient responses or adverse effects.
  • Assists with regulatory filings including IRB submissions.
  • May assist in enrolling human subjects.
  • Provides clerical and technical support to ensure adherence to protocols.

Skills

Database management
Regulatory compliance
Data collection
Documentation
Multitasking

Education

High School Diploma/GED

Tools

Database software
IRB submission systems

Job description

Jefferson Health is seeking staff to oversee day-to-day activities of clinical trials in accordance with Good Clinical Practice (GCP). The role involves data management, biospecimen processing, and clerical tasks to assist investigators with organizing and compiling clinical research data.

The position includes recruiting and consenting subjects, conducting study visits, and supporting regulatory submissions. Strong regulatory knowledge and ability to manage multiple tasks are required.

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