PRN Data Coordinator

🔥 7 minutes ago

🤠 Texas – Remote

🤠 Texas – Remote

💵 $14 - $28 / hour

⏱ Part Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Review study protocols for assigned studies • Ensure source-document data is accurately reflected on electronic or paper Case Report Forms • Track source documents filed into subject folders • Assist with reconciliation of study records for archive • Identify and report problems or potential problems to the supervisor • Request, schedule, and attend required training • Work under the general supervision and guidance of the Senior Manager, Study Conduct

🎯 Requirements

• Excellent written and oral communication skills • Ability to understand complex written and oral instructions • Basic computer knowledge and applications for business correspondence and electronic Case Report Form data entry • Strong interpersonal skills • Excellent attention to detail • Some knowledge of the clinical research process, including Good Clinical Practices • Bachelor’s degree or associate degree, preferably in Life Sciences or Health, and/or experience in a phase I clinical environment • Preferred: Experience or class work in the health field

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Transparent compensation and pay equity