Lead Clinical Data Programmer

September 15

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Clario

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Cardiac Solutions • Medical Imaging • eCOA • Respiratory Solutions • Precision Motion

1001 - 5000 employees

Founded 1973

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 Private Equity Round on 2019-10

Description

• Lead and Mentor a team of Clinical Data Programmers • Create and test SAS code used for standard and non-standard data file creation • Review Clario standard and non-standard data specifications • Attend client meetings to understand data collection requirements • Develop programs to create Clario standard and non-standard data files • Participate in the validation of encoding programs which generates CLARIO standard and non-standard data files • Performing ad-hoc programming activities utilizing raw data • Review User Requirements and create, review and approve Functional and Technical Specifications • Work with data management in providing programming support for DM activities • Prepare and participate in internal and external audits • Identify opportunities to improve the methodology and provide practical solutions • Contribute to the development of best practices to improve quality, efficiency and effectiveness • Organize team resources to meet client needs • Oversee training of new Clinical Data Programmers • Participate in new hire interviews and provide feedback to management

Requirements

• BS/BA Degree in Life Sciences or related field preferred or BS/BA Degree in computer sciences or related field • SAS ADVANCED certified • Ideally five or more years of experience in a pharmaceutical company or a CRO as a SAS Programmer • Experience in SAS/BASE, SAS/MACRO and SAS/SQL products and procedures • One or more years of experience in database design and data structures • Understanding of the pharmaceutical drug development process • Minimum of five years of experience in the pharmaceutical or healthcare industry • Strong organization, analytical and communication skills • Detail-oriented • Extensive experience in implementing CDISC SDTM and Define standards including EG, CO, DM, RE, VS, SUPP CDISC SDTM domains • Experience with Windows and Microsoft Office products preferred • Strong written and verbal communication skills • Fluency in English (spoken and written) • Experience with another programming languages is a plus • Proven experience working with large, complex real-world data sets (more specifically, patient data) • Knowledge of technical and regulatory requirements related to the role • Excellent time management skills, contributing to multiple projects with competing timelines • Leadership/Mentoring skills: Proven ability to motivate people, instill accountability and achieve results • Prior leadership experience a plus

Benefits

• Competitive compensation + commission scheme • Attractive benefits (security, flexibility, support and well-being) • Engaging employee programs • Technology for hybrid working and great onsite facilities