Clinical Data Programmer I

🕒 July 7

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Clario

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1973

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 Private Equity Round on 2019-10

Healthcare • Consulting • Logistics

Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.

📋 Description

• Develop and test SAS and/or Python programs to generate standard and non-standard clinical data files • Review and interpret data specifications, collaborating with Data Management to finalize requirements • Support the validation of encoding and programming outputs to ensure accuracy and compliance • Process data extracts and manage daily encoding requests to support ongoing study activities • Contribute to study archival processes and ensure data deliverables meet project timelines • Perform ad-hoc programming and data analysis activities, including quality control checks, data mining, and custom client requests • Participate in client meetings, as appropriate, to understand data collection and reporting requirements • Create and/or review functional and technical specifications based on user requirements • Partner with Data Management to support data review and issue resolution activities • Contribute to process improvements, SOP development, and documentation related to Clinical Data Programming • Assist with onboarding and training of team members, as needed

🎯 Requirements

• Bachelor’s degree in Life Sciences, Computer Science, or a related field preferred • SAS Base certification required • Experience developing programs using advanced SAS procedures; exposure to Python is beneficial • Understanding of database design, data structures, and clinical data workflows • Familiarity with the pharmaceutical drug development process • Experience working with CDISC SDTM standards and domains (e.g., EG, CO, DM, RE, VS, SUPP) • Strong analytical, problem-solving, and organizational skills • High attention to detail with a commitment to data quality • Effective written and verbal communication skills • Proficiency with Microsoft Office tools • Fluency in English (spoken and written)

🏖️ Benefits

• Competitive compensation and benefits package • Flexible remote working environment • Opportunities for career growth and exposure to multiple clinical modalities • A collaborative, global team focused on advancing clinical research