Regeneron Pharmaceuticals Inc.
Senior Statistical Programmer
Regeneron Pharmaceuticals Inc., Richmond, Virginia, United States,
The Senior Statistical Programmer provides support to the lead programmer and study team on all programming activities according to the study requirements and the timelines. This role contributes to studies in various therapeutical areas and all clinical trial phases. The incumbent implements and executes the programming and project standard under minimal supervision of the lead programmer and manager to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. Maintains programming documentations such as study tracker, code, logs, and outputs in a regulated environment.
In this role, a typical day might include the following:Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements.Assist in the coordination of activities and communicate shifting timelines and milestones.Integration of data across studies in support of CSS/CSE.Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies.Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports.If applicable, develop and provide department training for applications and standard tools developed by the department functions group.Provide programming support for simple presentations and basic statistical ad-hoc requests.Assist in the more complex data presentations.Demonstrate company values by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability.Create and maintain the programming specification and other documentation in accordance with SOPs/Guidance/WI/process to ensure traceability and regulatory compliance.This role may be for you if you have:Proficiency in SAS programming skills in a clinical data environment.Knowledge of other programming languages such as R, Python etc. is a plus.Good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles).Ability to work on global interdisciplinary teams.Good organizational, interpersonal, and communication skills.Positive attitude, team player and growth mindset.To be considered for this opportunity you will need:MS. (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 3+ (4+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.SAS Certification desirable.Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.Salary Range (annually) $90,700.00 - $148,100.00
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In this role, a typical day might include the following:Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements.Assist in the coordination of activities and communicate shifting timelines and milestones.Integration of data across studies in support of CSS/CSE.Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies.Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports.If applicable, develop and provide department training for applications and standard tools developed by the department functions group.Provide programming support for simple presentations and basic statistical ad-hoc requests.Assist in the more complex data presentations.Demonstrate company values by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability.Create and maintain the programming specification and other documentation in accordance with SOPs/Guidance/WI/process to ensure traceability and regulatory compliance.This role may be for you if you have:Proficiency in SAS programming skills in a clinical data environment.Knowledge of other programming languages such as R, Python etc. is a plus.Good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles).Ability to work on global interdisciplinary teams.Good organizational, interpersonal, and communication skills.Positive attitude, team player and growth mindset.To be considered for this opportunity you will need:MS. (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 3+ (4+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.SAS Certification desirable.Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.Salary Range (annually) $90,700.00 - $148,100.00
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