Principal Statistical Programmer- US Timings

1 week ago


London, Greater London, United Kingdom Tech Observer Full time
Tech Observer is a leading Global CRO headquartered in New Jersey, USA, with a presence in over 20 countries including India, Denmark, UK, and Singapore. We are currently looking to fill the following roles: FSP: - Statistical Programmers: Candidates with 5-8 years of experience in clinical SAS Programming - Senior Statistical Programmers: Candidates with 8-12 years of experience in clinical SAS Programming - Principal Statistical Programmers: Candidates with 12+ years of experience in clinical SAS Programming Location: United Kingdom (applicants eligible to work in the UK will be considered) Work Timings: Candidates should be available during US Timings (3 days EST and 2 days PST) Job Responsibilities: - Ensure compliance with working SOPs and adhere to Good Clinical Practice (GCP) guidelines - Implement and follow the latest CDISC, FDA Guidelines, and industry standards - Participate in the review of Case Report Forms, annotated CRFs, database structures, and study documentation - Review and interpret Report and Analysis Plans for assigned projects - Develop SAS programs for clinical trial data management and statistical analysis - Carry out electronic data transfer and develop programs for data review - Design utilities/SAS systems to support Clinical Data Management activities - Review production runs to ensure quality - Provide feedback for SOP improvement and ensure team quality - Act as Lead Programmer or Biometrics Project Manager when required - Offer support to senior Statistical Programming staff - Advise on project scope changes and decision-making - Encourage process improvement within the Statistical Programming group - Stay updated on programming and IT developments for clinical trial data management - Perform other duties as assigned by senior staff

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