In-house Clinical Research Associate II

🔥 0 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $50k - $99k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🦅 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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• Assist with feasibility questionnaires and CDA collection from potential sites • Coordinate study material shipment and receipt by study sites • Update and quality-review site-related documentation for filing in the Trial Master File (TMF) • Support field CRAs with Investigator Site File maintenance, TMF reconciliation, and TMF quality control • Conduct pre-study, study initiation, interim, remote monitoring, and close-out visits under guidance • Assist with investigational product inventory • Maintain regular communication with study sites • Complete remote review of electronic data capture (EDC) case report forms • Assist sites with resolution of EDC and vendor queries • Pull reports, maintain study trackers, and provide information to Clinical Trial Managers • Prepare field CRAs for visits by summarizing action items, protocol deviations, queries, supplies, and training needs • Assist with site staff changes, documentation, qualifications, training, and task delegation • Manage vendor access for site staff • Support prescreening, screening, and recruitment • Assist with Subject Eligibility Review tracking and support the Medical Monitor • Serve as operational point of contact for clinical research trials when applicable • Mentor and train In-house CRA I and II team members • Attend and present updates during study meetings • Perform other duties as assigned

🎯 Requirements

• Good oral and written communication skills • Good planning and organizational skills with effective time management • Good interpersonal skills • Ability to work in an organized and methodical manner • Good understanding of clinical research principles and process • Good understanding of FDA and/or EU Directive regulations, ICH Guidelines, and local regulatory requirements; training provided by WCT • Good understanding of standard operating procedures; training provided by Worldwide Clinical Trials • Basic knowledge of Microsoft Office • Familiarity with IVRS and eCRF systems; training provided by Worldwide Clinical Trials • A minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy, or other related science • A minimum of two years of clinical research experience (e.g., study coordinator, research nurse, etc.)

🏖️ Benefits

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