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Celerion

Global CRO for early-phase development

Data Programmer

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeBelfast, UKNo salary listed

About the Job

Requirements

  • A bachelor's degree with at least 1 year of programming experience, or comparable experience in a related industry.
  • Previous experience with SAS and clinical data is preferred.
  • Computer Science, Mathematics, or IT graduate applicants are also considered.
  • Demonstrated communication and interpersonal skills.
  • Demonstrated problem-solving and decision-making skills.
  • Demonstrated ability to manage multiple priorities.
  • Internal candidates with a strong clinical data review, data management, or IT background are also considered.

Responsibilities

  • Develop and support clinical database programming activities and associated documentation for clinical trial set-up, conduct, and close-out in line with protocol requirements, standard operating procedures, Good Clinical Programming Practices, Clinical Data Interchange Standards, and applicable sponsor or regulatory requirements.
  • Deliver and support all pre-database-lock SAS programming processes associated with data collection, reporting, and cleaning.
  • Support data import programming and reconciliation activities as needed.
  • Deliver and support raw/CDASH, lab-only, CDISC/SDTM, or sponsor-specified custom data transfers.
  • Participate in process-improvement initiatives.
  • Ensure data programming delivers quality outputs on time or earlier, following good programming practices and adequately documenting SAS code.

Desired Qualifications

  • Previous experience with SAS and clinical data is preferred.

About the Company

Celerion

Global CRO for early-phase development

Celerion is a global contract research organization focused on early-phase drug development. It conducts contracted research across clinical trial design, feasibility studies, project management, clinical and medical monitoring, bioanalytical sciences, and regulatory affairs, using High Resolution Mass Spectrometry-based metabolite profiling to inform decisions. Its advantage comes from over 40 years of experience, specialized metabolite profiling, and a global, integrated service model that accelerates development timelines. The goal is to help pharmaceutical and biotech clients bring safe and effective treatments to patients faster through rigorous, high-quality research.

Company size
1,001-5,000
Company stage
Acquired
Total funding
Not listed
Headquarters
Lincoln, NE
Founded
2010

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