Data Entry Coordinator - Clinical Trials (Growing Team)

Alcanza Clinical Research; Charleston (SC); On-site; USD 34,000 - 42,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

Health Savings Account

401(k) plan with safe harbor match

Job summary

Alcanza Clinical Research is seeking a Data Entry Coordinator at our Charleston, SC location. This role focuses on accurate data capture for clinical trials, ensuring entry into EDC and other systems with strict adherence to protocol guidelines and HIPAA requirements.

The position supports site activities within a collaborative environment, handling confidential information and maintaining data quality across multiple studies and phases.

Qualifications

• High School diploma or equivalent (required).
• 1+ year of clinical data entry or related experience preferred.
• Proficiency with Microsoft Office apps, email, and web tools.

Responsibilities

• Enter patient visit data into EDC and other systems accurately and timely.
• Review patient charts and medical records to ensure data accuracy per eCRF guidelines.
• Report irregularities or issues to study team and relevant parties.
• Support other clinical research activities as needed.
• Maintain confidentiality of patient, site, and company information in line with HIPAA and SOPs.

Skills

Typing 40+ wpm

Organizational skills

Written communication

Verbal communication

Interpersonal skills

Attention to detail

Multitasking

HIPAA compliance

Integrity and dependability

Education

High School diploma or equivalent

Tools

Microsoft Office

Email & web applications

Job description

Alcanza Clinical Research is seeking a Data Entry Coordinator at our Charleston, SC location. This role focuses on accurate data capture for clinical trials, ensuring entry into EDC and other systems with strict adherence to protocol guidelines and HIPAA requirements.

The position supports site activities within a collaborative environment, handling confidential information and maintaining data quality across multiple studies and phases.