eClinical Solutions is a clinical data management company that provides integrated data review and management solutions for the biotech and pharmaceutical industries. Their platform, elluminate, empowers organizations to modernize and automate their clinical data workflows, ensuring efficient data acquisition, management, and analysis. By leveraging advanced analytics and technology-driven approaches, eClinical Solutions helps streamline trial operations and improve productivity, enabling better decision-making in clinical research.
Clinical Data Management • EDC Services • Statistical Programming • Clinical Data Reporting and Analytics • Clinical Data Repository Development and Management
201 - 500 employees
Founded 2012
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
💰 Private Equity Round on 2020-01
February 27
eClinical Solutions is a clinical data management company that provides integrated data review and management solutions for the biotech and pharmaceutical industries. Their platform, elluminate, empowers organizations to modernize and automate their clinical data workflows, ensuring efficient data acquisition, management, and analysis. By leveraging advanced analytics and technology-driven approaches, eClinical Solutions helps streamline trial operations and improve productivity, enabling better decision-making in clinical research.
Clinical Data Management • EDC Services • Statistical Programming • Clinical Data Reporting and Analytics • Clinical Data Repository Development and Management
201 - 500 employees
Founded 2012
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
💰 Private Equity Round on 2020-01
• You will make an impact: Principal Clinical Database Programmers are operationally responsible to provide technical support and oversight for the Medidata Clinical Cloud (MCC) implementation activities. • Validates specification to development through leading team review, co-programmer review, and User Acceptance Testing • Responsible for the development, maintenance, and compliance of complete database builds and EDC standards in support of clinical studies including, but not limited to, Global Library, Edit Checks, CRF modules and Standard/Custom Reports • Functions as an EDC Subject Matter Expert (SME) providing guidance and best practice recommendations to Data Management, operations teams, and other stakeholders • May lead teams and/or supervise other programmers and serve in a project management capacity. • Support development and review of SOPs, and Work Guidelines to promote consistency and identify additional opportunities for standardization and departmental efficiency.
• Four-year college degree or higher preferred, analytic discipline a plus (Computer Science or Health related field) • 7+ years in Pharmaceutical/Biotechnology industry or equivalent, preferably in Services or Consulting role preferred • Ability to work creatively and independently to carry out assignments of a complex nature • Ability to communicate and work effectively and cooperatively with other professional staff members • Detail oriented, ability to multitask with strong prioritization, planning and organization skills • Excellent knowledge of English; verbal and written communication skills • Proficiency in Microsoft Office Applications, specifically MS Project and MS Excel • Experience with requirements gathering, design and specification development of CRFs, edit checks, site queries, and understanding of database structures and programming languages • Strong knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology preferred • Familiarity with Clinical Systems and technologies: ePRO, IVRS/IWRS, CTMS • Experience with Data Reporting Tools: Business Objects, JReview, Cognos, Crystal Reports or related preferred
• Accelerate your skills and career within a fast-growing company while impacting the future of healthcare. • eClinical is a winner of the 2023 Top Workplaces USA national award! • Our team seeks out opportunities to learn, grow and continuously improve. • Bring your authentic self, you are welcome here!
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