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Position: Principal Statistical Programmer
Institution: CSL Behring
Location: Cambridge, Massachusetts, United States
Duties: Direct the work of statistical programming services provided by vendors to achieve quality, timely, and cost-effective study deliverables; Participate in the development of and ensures compliance to Standard Operating Procedures (SOPs), policies, and guidelines; Perform statistical programming for clinical trial data analysis and reports; Assist to establish and implement programming standards and comply with regulatory requirements among project team members and across all studies; Review deliverables before transfer to either internal or external sources
Requirements: MS/PhD in Statistics (or equivalent), plus undergraduate degree in a quantitative field; At least 4 years of experiences in Clinical Development in a Pharmaceutical or Biotechnology setting; Experience in statistical programming projects in the pharmaceutical industry demonstrated by the ability to independently act as a statistical programmer for all phases of clinical trials; Experiences in SAS language procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH
   
Text: CSL Principal Statistical Programmer I Vereinigte Staaten von AmerikaR-1521550606 Seqirus Inc Stellenbeschreibung An exciting opportunity has arisen in our Clinical Development Division for a Senior Statistical Programmer who will be a member of the Biostatistics team and play an important role in performing specific statistical programming tasks required for clinical trial analysis and reporting. Reporting to the Associate Director, Clinical Standards and Programming, this position will work closely with other members of the BDPM on various clinical projects. The jobholder may function as Lead Statistical Programmer on a specific project and will have support responsibilities with potential for matrix management, participation in global teams, interacting with regulatory agencies in multiple countries. Your key accountabilities will include, but not limited to: Direct the work of statistical programming services provided by vendors to achieve quality, timely, and cost-effective study deliverables. Participate in the development of and ensures compliance to Standard Operating Procedures (SOPs), policies, and guidelines Perform statistical programming for clinical trial data analysis and reports Assist to establish and implement programming standards and comply with regulatory requirements among project team members and across all studies Review deliverables before transfer to either internal or external sources To be successful in this role, the jobholder will have: Education & Qualifications MS/PhD in Statistics (or equivalent), plus undergraduate degree in a quantitative field. Skills & Experience At least 4 years of experiences in Clinical Development in a Pharmaceutical or Biotechnology setting Experience in statistical programming projects in the pharmaceutical industry demonstrated by the ability to independently act as a statistical programmer for all phases of clinical trials. Experiences in SAS language procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH; Exhibit mastery of project management tasks and skills as related to statistical programming including teamwork, planning, organization, delegation, coordination, metrics, and oversight of contractors; Solid knowledge of CDISC standard and its implementation Demonstrate strong knowledge in medical terminology and clinical trial methodologies. Strong interpersonal and communication skills (verbal and written) bridging scientific and business needs - integrating quantitative sciences, strong drug development knowledge Fluent in English (oral and written). We want Seqirus to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces diversity, equity and inclusion. Learn more about Diversity, Equity & Inclusion at Seqirus. Do work that matters at Seqirus About Us Our Benefits Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join Seqirus. About Seqirus Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn more about Seqirus. We want Seqirus to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces diversity, equity and inclusion. Learn more about Diversity, Equity & Inclusion at Seqirus. Do work that matters at Seqirus! Teilen: RegionNord- und Südamerika Bundesstaat/ProvinzMassachusetts StadtCambridge Hausanschrift50 Hampshire Sreet Primary LocationSeqirus USA - MA - Cambridge Additional LocationsSeqirus Netherlands - Amsterdam;Seqirus USA - NJ - Summit Vollzeit/TeilzeitVollzeit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please click below. EEO Statement Präsentiert vonYello Diese Website verwendet Cookies, um Ihre Browsing Erfahrung zu verbessern. Weiter Surfen oder verwerfen diese Nachricht um zu akzeptieren. Finden Sie heraus mehr über unsere Cookie-Richtlinien hier.
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