Senior Manager, Statistical Programming

Regeneron Pharmaceuticals; Cambridge (MA); On-site; USD 150,500 - 245,500; Full time

Benefits offered by this job

Health and wellness programs

401(k) company match

Bonuses

Paid time off

Job summary

Regeneron Pharmaceuticals seeks a Senior Manager Statistical Programming to lead programming for clinical studies, ensuring alignment with project strategies and delivering statistical deliverables through regulatory approval, product launch, and annual reports. The role oversees internal teams and CROs, develops standards, and mentors staff.

The position is on-site in the United States and requires a Master’s degree with 8–10 years of relevant experience; SAS certification is desirable.

Qualifications

• Master's Degree and 8-10 years of relevant experience.
• SAS Certification desirable.

Responsibilities

• Independently coordinate and oversee preparation, execution, reporting and documentation of project analysis programming within a therapeutic area.
• Mentor junior level staff and develop collaborative work environment.

Skills

Statistical programming

Team leadership

Mentor junior staff

Education

Master's Degree

Tools

SAS

Job description

PLEASE NOTE THIS IS AN ONSITE POSITION AND NOT ELIGIBLE REMOTE.

A Senior Manager Statistical Programming provides timely support to the project team on all programming matters according to the project strategies within a therapeutic area. As an integral part of a project team, the incumbent provides project leadership and contributes to the programming support for processing data from clinical studies. Project requirements will be identified according to a Statistical Analysis Plan, programming specifications or user requirements/design documents using internal standards and guidelines. The incumbent is responsible for leading the programming aspect of the project, both internally or CROs, for all programming deliverables and participates in the identification and development of programming standards and macro development to facilitate the creation of statistical deliverables from a single study through to regulatory approval, product launch, and annual reports. May be asked to oversee special projects / work with clinical task force. Meets statistical adhoc requests of senior management.

Typical Day / Responsibilities

• Independently coordinate and oversee the preparation, execution, reporting and documentation of project analysis programming within a therapeutic area using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Manage and coordinate programming and QC of analysis datasets and TFLs following Regeneron standard data models and/o integration of data across studies in support of CSS/CSE and esub deliverables.
• Implement and mentor others on the use of department standardization tools or therapeutic area standard analysis when programming clinical data or system application deliverables.
• Contribute to programming development and quality control of the programming deliverables utilizing Regeneron tools and methodologies.
• Programming representative within a therapeutic area in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If applicable, programming representative for an application development to the user audience.
• Develop data models, programming standards and code, and train end users in the use of project standards to support programming deliverables that follow regulatory submission requirements.
• Mentor junior level staff in therapeutic area requirements. Develop collaborative work environment and be a positive role model.
• Advise all relevant employees about the procedures surrounding retention of data, records, and information for employees in their group.

Qualifications

• Master's Degree and 8-10 years of relevant experience.
• SAS Certification desirable.

Benefits

We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.

Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.

Equal Opportunity Employment

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.

Salary Range (annually)

$150,500.00 - $245,500.00