Clinical Data Entry Coordinator — Drive Impactful Trials

ActivMed Practices & Research, LLC.; Decatur (GA); On-site; USD 32,000 - 46,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

Health Savings Account

401k with match

Job summary

Alcanza Clinical Research is seeking a Data Entry Coordinator to support clinical studies across our national network. You will enter visit data into eDC and related systems, ensure accuracy, and help maintain regulatory compliance under GCP/ICH/HIPAA.

The role requires meticulous attention to detail, fast typing (40+ wpm), and the ability to work both independently and with a team. Full-time positions offer comprehensive benefits including medical, dental, and vision insurance, life and

Qualifications

• High school diploma or equivalent with 1 year of clinical data entry experience.
• Proficient typing 40+ wpm and accurate data entry.
• Strong organization and attention to detail.
• Excellent written and verbal communication abilities.
• Able to work independently and with team members.
• Maintain HIPAA confidentiality and comply with regulations.
• Full-time benefits eligibility begins on day one.

Responsibilities

• Enter patient data into eDC and other data systems for clinical trials.
• Review patient charts and records for accuracy and protocol compliance.
• Report irregularities or problems to appropriate parties.
• Support other clinical research-related activities as needed.
• Ensure compliance with SOPs, regulations, ICF documentation, and GCP/GDP guidelines.
• Maintain confidentiality of patients, customers, and company information.

Skills

40+ wpm typing

Organizational skills

Written & verbal communication

Interpersonal skills

Multitasking

Integrity & dependability

HIPAA compliance

Team collaboration

Education

High school diploma or equivalent

Tools

Microsoft Office

eDC systems

Web applications

Job description

Alcanza Clinical Research is seeking a Data Entry Coordinator to support clinical studies across our national network. You will enter visit data into eDC and related systems, ensure accuracy, and help maintain regulatory compliance under GCP/ICH/HIPAA.

The role requires meticulous attention to detail, fast typing (40+ wpm), and the ability to work both independently and with a team. Full-time positions offer comprehensive benefits including medical, dental, and vision insurance, life and