Senior Clinical Research Associate – Contract Position

🔥 17 hours ago

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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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ProTrials Research Inc.

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

ProTrials Research Inc. is a clinical research organization (CRO) headquartered in the United States, offering a wide range of services to the pharmaceutical, biotechnology, and medical device industries. The company provides quality-driven site management, clinical monitoring, project management, data management, and supportive clinical development services. With a focus on therapeutic areas such as oncology, ophthalmology, central nervous system, infectious diseases, women's health, and medical devices & diagnostics, ProTrials is dedicated to delivering high-quality clinical research. Their services include project management, clinical operations, quality assurance, medical and regulatory support, and they also act as a functional service provider, emphasizing virtual trials and remote monitoring capabilities.

📋 Description

• Monitor clinical studies of investigational and approved products, including qualification, initiation, interim, and close-out site visits • Manage and train site personnel on therapeutic area, protocol requirements, source documentation, and case report form completion • Manage and track preparation and return of investigational supplies at individual sites • Monitor and document investigational product dispensing, inventory, and reconciliation • Monitor and document laboratory sample storage and shipment • Monitor and report site enrollment and termination updates, monitoring visits, protocol deviations/exceptions, serious adverse events, and laboratory abnormalities • Review source data and case report forms for accuracy, completeness, and integrity; identify and resolve data issues • Review data queries and listings and work with study centers to resolve discrepancies • Review regulatory documentation and support study centers with regulatory issues • Maintain complete and accurate study files and verify required documentation • Maintain timely contact with study centers, investigators, coordinators, client personnel, and other clinical-trial stakeholders • Support CRA I and CRA II staff by providing solutions to resolve issues

🎯 Requirements

• RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training, and previous CRA experience demonstrating career growth in the CRA position • Detail-oriented • Excellent organizational skills, strong interpersonal and communications skills, and strong problem-solving skills • Flexibility with changing priorities • Ability to efficiently perform and prioritize multiple tasks • Familiarity with the medical and pharmaceutical industries, and related terminology and practices • Extensive knowledge of FDA regulations and their practical implementation • Ability to travel, including by air or by car on short notice • Proficiency in Microsoft Word, Excel, and PowerPoint

🏖️ Benefits

• Equal opportunity employer committed to a workplace free from discrimination and harassment