As a Statistical Programmer, your role involves applying technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams. You will work with limited supervision early in your role and independently later on. Your key responsibilities include:
Ensuring excellence in the programming of analysis-ready datasets, tables, listings, and figures. - Being accountable for the quality and timely delivery of datasets and displays required for clinical study reports. - Ensuring appropriate documentation and quality control across the lifespan of the study for all your programming deliverables. - Exhibiting routine and occasionally complex problem-solving skills. - Working with statisticians and programming leads to ensure clear specifications for your programmed deliverables. To be successful in this role, you should possess the following qualifications and skills:
Bachelor or Master's (preferred) Degree in Statistics, Biological Sciences, IT, or a related field. - 8-15 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency. - Hands-on experience in Statistical Programming and SAS. - Expertise in clinical trials with an understanding of data operations required for reporting clinical trial data. - Good understanding of ICH and regulatory guidelines. - Working knowledge of clinical data and relevant data standards. - Strong written and oral communication skills, and project management skills. - Proven ability to operate with limited oversight. - Knowledge of at least 1 Therapeutic Area. - Proven ability to manage delivery under tight timelines. - CDISC experience is desirable. As a Statistical Programmer, your role involves applying technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams. You will work with limited supervision early in your role and independently later on. Your key responsibilities include:
Ensuring excellence in the programming of analysis-ready datasets, tables, listings, and figures. - Being accountable for the quality and timely delivery of datasets and displays required for clinical study reports. - Ensuring appropriate documentation and quality control across the lifespan of the study for all your programming deliverables. - Exhibiting routine and occasionally complex problem-solving skills. - Working with statisticians and programming leads to ensure clear specifications for your programmed deliverables. To be successful in this role, you should possess the following qualifications and skills:
Bachelor or Master's (preferred) Degree in Statistics, Biological Sciences, IT, or a related field. - 8-15 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency. - Hands-on experience in Statistical Programming and SAS. - Expertise in clinical trials with an understanding of data operations required for reporting clinical trial data. - Good understanding of ICH and regulatory guidelines. - Working knowledge of clinical data and relevant data standards. - Strong written and oral communication skills, and project management skills. - Proven ability to operate with limited oversight. - Knowledge of at least 1 Therapeutic Area. - Proven ability to manage delivery under tight timelines. - CDISC experience is desirable.