Clinical Trials Data Entry Coordinator

ActivMed Practices & Research, LLC.

Charleston (SC)

On-site

USD 42,000 - 54,000

Full time

5 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Life insurance
Short/Long-term disability insurance
Health Savings Account
401k plan with safe harbor match

Job summary

Alcanza Clinical Research is seeking a Data Entry Coordinator to ensure accurate entry of clinical visit data into EDC and related systems. You will collaborate with site team members to maintain data integrity and regulatory compliance.

The role requires a High School diploma or equivalent and at least 1 year of clinical data entry experience, with strong typing (40+ wpm), organization, and communication skills.

Qualifications

  • Minimum of 1 year of clinical data entry experience.
  • Proficiency with computer applications and ability to type proficiently (40+ wpm).
  • Strong organizational and detail orientation are essential.
  • Great written and verbal communication, and ability to work independently and with others.

Responsibilities

  • Enter patient data into eDC and other data systems accurately and timely.
  • Review charts and records to ensure data are entered per eCRF guidelines.
  • Report irregularities or problems with a study to appropriate parties.
  • Support other clinical research activities as needed.
  • Maintain compliance with SOPs, regulations, ICF documentation, and GCP/GDP guidelines.
  • Maintain confidentiality of patients, customers, and company information.

Skills

Typing 40+ wpm
Data entry
Attention to detail
Written and verbal communication
Multitasking
HIPAA compliance awareness
Professional conduct
Confidentiality

Education

High School diploma or equivalent

Tools

Microsoft Office
Email
Web applications

Job description

Alcanza Clinical Research is seeking a Data Entry Coordinator to ensure accurate entry of clinical visit data into EDC and related systems. You will collaborate with site team members to maintain data integrity and regulatory compliance.

The role requires a High School diploma or equivalent and at least 1 year of clinical data entry experience, with strong typing (40+ wpm), organization, and communication skills.

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