Study Design Specialist

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $60k - $70k / year

⏰ Full Time

🟢 Junior

✍️ Designer

🚫👨‍🎓 No degree required

👻 Ghost score 2%

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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CRIO

WebsiteLinkedInAll Job Openings

51 - 200 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $9M Series B on 2022-01

Healthcare • Consulting • Logistics

CRIO is a company that provides an all-in-one platform for clinical research operations, focusing on improving protocol compliance, eliminating transcription tasks, and saving time and money for sites and sponsors. CRIO's solutions support single sites, networks, academic research, and sponsors, offering products like eSource, eConsent, medical record APIs, and site CTMS, among others. The company emphasizes innovation, collaboration, and efficiency, with tools that enhance clinical trial site operations and promote diversity in clinical research. CRIO partners with other companies to drive innovation within the industry, and their platform is widely used for its reliability and ease of use in clinical settings.

📋 Description

• Create comprehensive study builds from start to finish in the CRIO platform • Develop eSource from protocols and eCRFs • Conduct post-build quality control reviews • Configure budgets in the CRIO finance module • Utilize protocols, eCRF guidelines, pharmacy manuals, lab manuals, and other source documents to produce comprehensive builds for clients • Interpret Clinical Trial Agreements and budgets for configuration in the CRIO finance module • Design visit schedules and procedures for CTMS-only studies • Complete client-requested edits and customizations • Provide quality control reviews of client-built eSource and budget templates • Manage complex trials to ensure all data is captured appropriately • Modify standard templates to comply with protocol requirements • Complete assignments on time • Mentor and train current and new CRIO employees

🎯 Requirements

• Experience with eSource, budget, and QC design in CRIO or other eSource/CTMS systems • BS in medical or sciences field (preferred qualification) • At least 1 year of healthcare experience • Ability to interpret clinical trial protocols, source documents, and clinical trial agreements • Knowledge of medical terminology and procedures • Experience tracking study financials • Strong people skills • Detail-oriented with solid time management skills • Well-organized, capable of establishing priorities, and executing tasks efficiently

🏖️ Benefits

• Work from anywhere (US based) • Unlimited PTO • 401k company match • Healthcare • Dental • Vision (Company Paid 100%) • Life insurance • Professional Development Reimbursement • Work From Home Expense Reimbursement • Occasional travel may be required based on business needs • Some flexibility in working hours may be needed to accommodate project schedules or time zone differences