Clinical Data Reviewer

Job not on LinkedIn

🕒 October 6

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟢 Junior

🟡 Mid-level

🔍🏥 Medical Reviewer

👻 Ghost score 15%

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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ALLEN SPOLDEN

WebsiteLinkedInAll Job Openings

51 - 200 employees

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Healthcare • Consulting • Manufacturing

ALLEN SPOLDEN is a workforce solutions provider specializing in talent and research solutions for the pharmaceutical, biotech, healthcare, and public health sectors. They offer services including functional service provider (FSP) solutions, data management, regulatory affairs guidance, and tailored staffing services to meet the specific needs of clinical research projects. Their expertise is aimed at driving efficiency, enhancing productivity, and ensuring compliance throughout clinical trial operations.

📋 Description

• Review clinical and laboratory data for accuracy, consistency, and completeness • Identify discrepancies requiring clarification from study sites • Apply clinical, laboratory, or patient-care knowledge to identify implausible or inconsistent data • Write and issue data queries to sites using provided guidelines and templates • Cross-check data across lab results, concomitant medications, adverse events, and medical history • Review medical coding with guidance from senior reviewers • Flag data quality trends, protocol compliance issues, and training needs • Support audit readiness by following SOPs and maintaining accurate documentation • Participate in Protocol Deviation, Data Review and Quality Team (DRQT), and Safety Monitoring Team (SMT) meetings • Assist with listings, trackers, and slides for data review meetings

🎯 Requirements

• Educated to Associate or Bachelor's level, or hold a diploma or certificate with relevant hands-on experience, in a life sciences, laboratory, or allied health field • 0-2 years of experience in a clinical, laboratory, dental, or healthcare setting, including internships, clinical placements, or externships • Comfortable reading and interpreting patient data such as vital signs, lab values, medication and allergy lists, treatment or procedure notes, or charts • Familiar with medical terminology and accurate documentation practices • Clear communicator in written and spoken English, with strong attention to detail • Organized, able to track multiple tasks and meet deadlines • Proficient in MS Excel and Office tools • Relevant certification or licensure is nice to have • Experience with EHR/EMR, practice management, or LIMS systems is nice to have • Interest in oncology or other specialty areas is nice to have

🏖️ Benefits

• Training provided in clinical trial processes, clinical database navigation, query writing, and medical coding • Mentorship as you build confidence • Remote work arrangement