The Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal partnering functions, collaborators, and external functional service providers to ensure all the programming results are delivered in a timely manner with high quality.
In this role, a typical day might include the following:
Lead programming support within multiple studies/projects in various study activities to ensure timely and high-quality programming deliverables in assigned projects and areas. Develop and maintain programming documentation and specifications following programming standards and processes.
Demonstrate company values by showing excellence, competence, collaboration, innovation, respect, ownership, and accountability.
Understand the scope of work, plan and complete the deliveries and timelines with the study team, programming lead, and management.
Support global regulatory authority submissions including preparing programming deliverables for submission and working closely with partnering functions to address health authority requests.
This role may be for you if you have: Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. 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). Knowledge of regulatory submissions and requirements is a plus.
SAS (Base, Stat, Macro, Graph); SAS certificates are a plus.
To be considered for this opportunity you must have:
MS (or BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical, or health-related industry.
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.
Salary Range (annually)
$106,200.00 - $173,200.00 #J-18808-Ljbffr
In this role, a typical day might include the following:
Lead programming support within multiple studies/projects in various study activities to ensure timely and high-quality programming deliverables in assigned projects and areas. Develop and maintain programming documentation and specifications following programming standards and processes.
Demonstrate company values by showing excellence, competence, collaboration, innovation, respect, ownership, and accountability.
Understand the scope of work, plan and complete the deliveries and timelines with the study team, programming lead, and management.
Support global regulatory authority submissions including preparing programming deliverables for submission and working closely with partnering functions to address health authority requests.
This role may be for you if you have: Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. 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). Knowledge of regulatory submissions and requirements is a plus.
SAS (Base, Stat, Macro, Graph); SAS certificates are a plus.
To be considered for this opportunity you must have:
MS (or BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical, or health-related industry.
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.
Salary Range (annually)
$106,200.00 - $173,200.00 #J-18808-Ljbffr
