Senior Clinical Database Programmer – LATAM

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Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 $35.2M Venture Round on 2021-03

Biotechnology • Healthcare Insurance • Pharmaceuticals

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Lead the development, testing, implementation, and support of clinical databases from start-up through post-lock • Guide database design, oversee programming activities, troubleshoot complex technical issues • Support system administration, forecast project needs, and contribute to SOP and process development • Provide leadership for cross-functional and organization-wide initiatives • Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues

🎯 Requirements

• Minimum 5 years’ experience • Bachelors and/or a combination of related experience • Professional working proficiency in English required • Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook • Able to handle a variety of clinical research tasks • Experience in Object Oriented Programming (C#, C++, VBS, etc.…) • Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.) • Experience in clinical database management system development • Experience in a clinical, scientific or healthcare discipline • Proficiency in more than one CDMS system to include building forms, edit checks and complex rule development • Awareness of CRF standards and input to maintenance of standards library • Ability to troubleshoot and support peers with technical issues and build solutions • Broad knowledge of drug, device and/or biologic development and effective data management practices • Strong leadership and interpersonal skills.

🏖️ Benefits

• Mentoring junior programmers • Training end users • Support onboarding • Technical leadership