Data Coordinator

🔥 3 minutes ago

🌐 Bulgaria, Slovakia, +1 more countries – Remote

🇧🇬 Bulgaria – Remote 🇸🇰 Slovakia – Remote 🇷🇴 Romania – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Data Coordinator

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Just posted.
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• No salary listed.

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Premier Research

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

💰 Venture Round on 2016-10

Healthcare • Consulting • Biotechnology

Premier Research is a company dedicated to helping biotech companies transform groundbreaking scientific ideas into life-changing medical treatments. They specialize in clinical research and development, product development and regulatory consulting, and offer expertise in areas such as oncology, hematology, rare diseases, cell and gene therapy, and pediatrics, among others. Premier Research is committed to boosting clinical development strategies and guiding innovations from molecule to market. They provide a range of services that support biotech firms in navigating the complex path to medical approval, with a focus on rare diseases and innovative therapies.

📋 Description

• Prepare documentation, including CCGs, Data Management Plans, Data Report Specifications, and External Data Transfer Specifications • Assist with developing standard test data and provide feedback on testing results • Perform user acceptance testing on studies, including edit-check testing • Maintain databases and support database updates • Perform data entry • Generate reports for data review • Review CRFs, data listings, and databases for protocol and documentation compliance • Generate queries to internal or external personnel to resolve problematic data • Review query responses and resolve discrepancies • Perform external data and serious adverse event reconciliation • Act as Lead Data Coordinator and/or Safety Reviewer on multiple studies • Submit documents to the Trial Master File (TMF) • Support TMF Quality Control activities • Perform database QC activities • Perform QC of study reports and CRF archive files • Support Data Scientists and/or Project Managers with financial project statistics, study metrics, dashboard updates, and project status reporting

🎯 Requirements

• Bachelor’s Degree or above (preferably in a Life Science) • 2–4 years of DM mastery or related clinical research industry experience • Knowledge of at least one Clinical Data Management System (CDMS), e.g. Medidata Rave or Calyx EDC • Fluent in English (written and spoken) • Strong analytical, investigative, and problem-solving skills • Proven ability to learn, navigate, and leverage new systems quickly • Exceptional organizational skills and high attention to detail • Customer-service mindset • Ability to multitask and balance competing priorities in a fast-paced environment

🏖️ Benefits

• Flexibility and balance to support employees’ lives • Skills and opportunities for professional growth and development

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