CDM Programmer II

Job not on LinkedIn

2 days ago

🌲 North Carolina – Remote

Although this job is listed in North Carolina, this company may be open to hiring remote in other states.

💵 $75.9k - $126.5k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🖥 Software Engineer

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Thermo Fisher Scientific

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Biotechnology • Pharmaceuticals • Science

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

10,000+ employees

Founded 1956

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

📋 Description

• Perform tasks following within the timelines established by the team, in accordance with the process outlined in the departmental procedures and indicated by the project contract. • Design, build and test project databases and edit checks. • Define and import data into the system. • Define, create and test listings for data review and perform programming activities in line with project requirements. • Act as the lead on studies of simple to moderate complexity with close supervision. • Research and leverage resources to resolve issues and manage moderately complex tasks through the development and application of new knowledge and professional skills in areas including programming and technology. • Participate in process improvement initiatives to increase efficiencies. • Increase knowledge and skills to gain good understanding of the lead programmer roles and overall department processes. • Ensure adherence to departmental working practice documents and SOPs, and contribute to the development of informal training materials.

🎯 Requirements

• Bachelor’s degree in Health Informatics, Bioinformatics, Data Science, Information Systems, or related field and two (2) years of experience as a CDM Programmer II, Clinical Data Programmer, involving clinical trial data programming, or related role involving clinical trial data programming. • Must have two (2) years of experience with: • Programming languages: SAS, SQL, C#; • Relational database systems (RDBMS) and structure: Oracle, MySQL; • SAS software modules: Base SAS, SAS/STAT, SAS/GRAPH, SAS macro, SAS ODS, SAS SQL; • SQL, Crystal Reports, and JReview; • Microsoft Word to produce relevant study documentation; • Microsoft Excel to manage and exchange study data; • Microsoft Project to manage timelines and resourcing of projects. • Must have one (1) year of experience with: • CDMS Clinical Data Management Systems: Medidata Rave, Veeva CDMS, Oracle Inform.