Clinical Data Coordinator — Ensure Accurate Trial Data

Worldwide Clinical Trials; United States; On-site; USD 41,328,000 - 82,656,000; Part time

Job summary

Worldwide Clinical Trials is seeking a PRN Data Coordinator to ensure accurate transcription of source data into the Case Report Form (CRF) in line with Good Clinical Practice. The role reports to the Senior Manager, Study Conduct and requires a Life Sciences or Health degree, with Phase I experience preferred.

Responsibilities include reviewing study protocols, reflecting data on CRFs (electronic or paper), tracking source documents, and assisting with archiving reconciliation.

Qualifications

• Bachelor’s degree in Life Sciences or Health preferred.
• Experience in a phase I clinical environment.
• Knowledge of Good Clinical Practice (GCP).
• Strong written and oral communication skills.

Responsibilities

• Review study protocol for assigned studies.
• Ensure source data is accurately reflected on the CRF (electronic or paper).
• Keep track of source documents filed into subject folders.
• Assist with reconciliation of study records for archive.
• Identify problems or potential problems and report them to supervisor.
• Attend any required training for this position.

Skills

Communication skills

Attention to detail

Data entry

eCRF systems

GCP knowledge

Education

Bachelor's or associate degree in Life Sciences or Health

Tools

eCRF systems

Job description

Worldwide Clinical Trials is seeking a PRN Data Coordinator to ensure accurate transcription of source data into the Case Report Form (CRF) in line with Good Clinical Practice. The role reports to the Senior Manager, Study Conduct and requires a Life Sciences or Health degree, with Phase I experience preferred.

Responsibilities include reviewing study protocols, reflecting data on CRFs (electronic or paper), tracking source documents, and assisting with archiving reconciliation.