PRN Clinical Data Coordinator for Trials

Worldwide Clinical Trials; Town of Texas (WI); On-site; USD 20,000 - 40,000; Part time

Benefits offered by this job

Competitive benefits package

Job summary

Worldwide Clinical Trials in the United States is seeking a PRN Data Coordinator to ensure accurate transcription of source data into Case Report Forms (CRFs) in alignment with Good Clinical Practice. You will work under supervision to maintain data integrity for clinical trials.

Responsibilities include reviewing study protocols, tracking source documents, and reconciling records for archive, while coordinating required trainings and maintaining clear communication with the study team.

Qualifications

• Bachelor’s degree in Life Sciences or Health or related field.
• Experience in a phase I clinical environment is preferred.
• Strong written and verbal communication skills required.

Responsibilities

• Review study protocol for assigned studies.
• Ensure source data is accurately reflected on CRFs (electronic or paper).
• Track source documents filed into subject folders.
• Assist with reconciliation of study records for archive.
• Identify problems and report to supervisor.
• Arrange and attend required trainings.

Skills

Communication skills

Attention to detail

Basic computer skills

Life sciences knowledge

Team collaboration

Education

Bachelor’s or Associate degree in Life Sciences/Health

Experience in Phase I clinical environment

Tools

eCRF software

EDC/Data entry tools

MS Office

Job description

Worldwide Clinical Trials in the United States is seeking a PRN Data Coordinator to ensure accurate transcription of source data into Case Report Forms (CRFs) in alignment with Good Clinical Practice. You will work under supervision to maintain data integrity for clinical trials.

Responsibilities include reviewing study protocols, tracking source documents, and reconciling records for archive, while coordinating required trainings and maintaining clear communication with the study team.