Company Detail

Celerion
Member Since,
Login to View contact details
Login

About Company

Job Openings

  • Remote Senior Data Analyst (Statistical Programming)  

    - Greater Manchester
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less
  • Remote Senior Data Analyst (Statistical Programming)  

    - Lisburn and Castlereagh
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less
  • Remote Senior Data Analyst (Statistical Programming)  

    - Highland Council
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less
  • Remote Senior Data Analyst (Statistical Programming)  

    - East Sussex
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less
  • Remote Senior Data Analyst (Statistical Programming)  

    - Bournemouth
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less
  • Remote Senior Data Analyst (Statistical Programming)  

    - Aberdeen City
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less
  • Remote Senior Data Analyst (Statistical Programming)  

    - Oxfordshire
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less
  • Remote Senior Data Analyst (Statistical Programming)  

    - Greater London
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less
  • Remote Senior Data Analyst (Statistical Programming)  

    - Derby
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less
  • Remote Senior Data Analyst (Statistical Programming)  

    - South Yorkshire
    Senior Data Analyst (Statistical Programming) Celerion is committed to... Read More
    Senior Data Analyst (Statistical Programming) Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role Celerion is seeking a Senior SAS Data Analyst to join our Data Management and Biometrics team in Belfast, Northern Ireland to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data. The Primary Responsibilities of this Position Are: - Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures. - Perform peer QC, double programming and validation functions for statistical outputs from studies. - Lead statistical programming activities on studies and deliverables. - Assist Management and Biostatisticians with complex projects. - Design and implement SAS programs for standardized use. - Train and mentor junior programmers. - Ensure compliance with statistical analysis plan and departmental procedures. Requirements Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field. 4+ years of SAS® programming experience in a CRO or Pharmaceutical industry. Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS. Experience applying CDISC requirements to generate ADaM datasets and supporting documentation ( define.xml , Reviewer’s Guides), demonstrating proficiency in these areas. Excellent interpersonal skills. Strong problem-solving and decision-making abilities. Demonstrates a high level of attention to detail. Demonstrated ability to work collaboratively as part of a team. Familiarity with R, Python, and other programming languages preferred. Celerion are an equal opportunities employer Read Less

Company Detail

  • Is Email Verified
    No
  • Total Employees
  • Established In
  • Current jobs

Google Map

For Jobseekers
For Employers
Contact Us
Astrid-Lindgren-Weg 12 38229 Salzgitter Germany