Clinical Data Quality Specialist

Celerion

Tempe (AZ)

In loco

USD 24.000 - 35.000

Tempo pieno

14 giorni+

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

Supera i filtri ATS

Descrizione del lavoro

Celerion in Tempe, AZ is seeking a detail-oriented QC/Data Entry associate to review source data and ensure accurate CRF data entry for regulatory reporting. You will support study setup, data cleaning, and ongoing QC activities in a fast-paced clinical trials environment.

Requirements include a High School Diploma or GED, 1–2 years of relevant experience, proficiency with MS Office, and strong written and verbal communication. Attention to detail and multi-tasking are essential to succeed.

Competenze

  • Minimum education: High School Diploma or GED.
  • 1–2 years industry experience preferred.
  • Previous QC/Data Entry or related experience preferred.
  • Medical Terminology Training preferred.
  • Excellent oral and written communication skills.
  • Ability to organize and manage multiple priorities.
  • Experience with complex processes and defined criteria.
  • Excellent time management skills required.

Mansioni

  • Attend study setup meetings to determine QC criteria and timelines.
  • Review study-specific source documents for accuracy and protocol conformity.
  • Ensure QC reviews are completed on time per study timelines.
  • Review source data for completeness and adherence to GCP/FDA guidelines.
  • Perform accurate data entry and verification for EC/CRFs.
  • Archive source documentation including CRFs.
  • Complete QC/DE milestones in a timely manner.
  • Perform standard quality control steps.

Conoscenze

Attention to detail
Oral and written communication
Time management
Organizational skills
MS Office proficiency

Formazione

High School Diploma or GED

Strumenti

MS Office

Descrizione del lavoro

Celerion in Tempe, AZ is seeking a detail-oriented QC/Data Entry associate to review source data and ensure accurate CRF data entry for regulatory reporting. You will support study setup, data cleaning, and ongoing QC activities in a fast-paced clinical trials environment.

Requirements include a High School Diploma or GED, 1–2 years of relevant experience, proficiency with MS Office, and strong written and verbal communication. Attention to detail and multi-tasking are essential to succeed.

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