Clinical Data Entry Coordinator — Precision & Compliance

Alcanza Clinical Research

Jacksonville (FL)

On-site

USD 22,000 - 30,000

Full time

5 days ago
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Benefits offered by this job

Health insurance
401k with safe harbor match
Dental and vision coverage

Job summary

Alcanza Clinical Research in Jacksonville, FL is seeking a Data Entry Coordinator to ensure accurate entry of clinical visit data into EDC and other data systems in compliance with GCP, ICH, HIPAA, FDA regulations, and SOPs.

You will review patient charts, support data management activities, and help maintain data quality and confidentiality across studies. A high school diploma and 1 year of clinical data entry experience are required, along with strong typing skills and attention to detail.

Qualifications

  • High School diploma or equivalent with 1 year of clinical data entry experience.
  • Proficiency with Microsoft Office, email, and web applications; typing 40+ wpm.
  • Strong organizational skills and attention to detail.
  • Excellent written and verbal communication.
  • Ability to handle confidential information per HIPAA.

Responsibilities

  • Enter clinical visit data into EDC and other systems.
  • Review patient charts and records for timely data entry.
  • Report irregularities to appropriate parties.
  • Support other clinical research activities.
  • Ensure compliance with SOPs, regulations, ICF, and GCP/GDP guidelines.
  • Maintain confidentiality of patients and company information.

Skills

Typing 40+ wpm
Strong organizational skills
Written & verbal communication
Interpersonal skills
Multitasking
Professional & ethical conduct
HIPAA compliance
Attention to detail
Self-motivated

Education

High School diploma or equivalent

Job description

Alcanza Clinical Research in Jacksonville, FL is seeking a Data Entry Coordinator to ensure accurate entry of clinical visit data into EDC and other data systems in compliance with GCP, ICH, HIPAA, FDA regulations, and SOPs.

You will review patient charts, support data management activities, and help maintain data quality and confidentiality across studies. A high school diploma and 1 year of clinical data entry experience are required, along with strong typing skills and attention to detail.

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