
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.
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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.
• Prepare clean databases by reviewing clinical trial data through CDMS or external data listings • Ensure captured data follows protocol and Data Management Plan rules • Provide input to and review Data Management Plans for clinical study deliverables • Generate queries to internal or external personnel to resolve problematic data • Review query responses, resolve discrepancies, and modify databases accordingly • Support development of CRFs and edit check specifications per protocol • Participate in user acceptance testing of CRFs and associated edit check specifications • Assist with user acceptance testing for study-specific data listings • Prepare and maintain documentation for CRF, edit check, and data listing testing, including follow-up testing
• Bachelor degree, or international equivalent from an accredited institution, preferably in a technical, clinical, or health-related field, or equivalent combination of education, training and experience • 3 to 5 years of practical experience using commercial clinical data management systems and/or EDC products (e.g., Oracle RDC / Inform, Medidata Rave, DataLabs, etc.) • Alternatively, proven experience in all primary job functions • Excellent English verbal and written communication skills • Excellent computer skills in a Microsoft Windows environment • Proficiency in Microsoft Office Suite tools, including Outlook, Word, and Excel • Proven ability to drive a successful customer experience through positive customer interactions, quality and timely deliverables, and task ownership • Strong analytical and organizational skills • Ability to work independently and manage multiple projects simultaneously in a fast-paced environment with changing priorities
• Health insurance (Doverie) • 23 days of annual leave • Food vouchers • Additional payment for internet (all remote employees are eligible) • Employee Assistance Program • Innovative technologies • Continuous learning
Apply Now🕒 July 29
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