Clinical Research Coordinator — Trials & Data Management

Socket.dev

Largo (FL)

On-site

USD 52,000 - 72,000

Full time

4 days ago
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Job summary

Socket.dev is seeking a Clinical Research Coordinator to support the administration of clinical trials. You will handle patient visits, data collection, and adherence to study protocols under supervision.

The role requires collaboration with investigators and sponsors, maintaining essential documents and ensuring compliance with HIPAA and GCP. A high school diploma is required, and a bachelor’s degree is preferred for this position.

Qualifications

  • Knowledge of medical terminology and good clinical practice.
  • Ability to manage high volumes of work with accuracy and timelines.
  • Experience with data collection and source documentation is preferred.

Responsibilities

  • Provide subject care and data collection procedures in line with study protocol and GCP.
  • Screen and identify potential subjects for inclusion per protocol criteria.
  • Coordinate and manage the clinical trial, communicate with sponsor and authorities, coordinate visits.

Skills

Attention to detail
Team collaboration
Data collection
Communication skills

Education

High School Diploma
Bachelor's degree preferred

Tools

EPIC software

Job description

Socket.dev is seeking a Clinical Research Coordinator to support the administration of clinical trials. You will handle patient visits, data collection, and adherence to study protocols under supervision.

The role requires collaboration with investigators and sponsors, maintaining essential documents and ensuring compliance with HIPAA and GCP. A high school diploma is required, and a bachelor’s degree is preferred for this position.

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