We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables ...
We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables ...
We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables ...
We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables ...
Senior Manager, Statistical Programming Department: Clinical Data Sciences & Analytics Reports To: Head of Statistical Programming Location: South San Francisco, CA or Princeton, NJ - On-site 4 days ...
Senior Manager, Statistical Programming Department: Clinical Data Sciences & Analytics Reports To: Head of Statistical Programming Location: South San Francisco, CA or Princeton, NJ - On-site 4 days ...
We are seeking a Senior Manager, Statistical Programming to join our Statistical Programming function, providing technical leadership across project teams within one or more therapeutic areas. In ...
We are seeking a Senior Manager, Statistical Programming to join our Statistical Programming function, providing technical leadership across project teams within one or more therapeutic areas. In ...
We are seeking a Senior Manager, Statistical Programming to join our Statistical Programming team, supporting a therapeutic area across our clinical portfolio. In this role, you will provide ...
We are seeking a Senior Manager, Statistical Programming to join our Statistical Programming team, supporting a therapeutic area across our clinical portfolio. In this role, you will provide ...
Director, Statistical Programming
$242K - $293K/yr
In this role, Cluster Head, is responsible for managing employees: set objectives, manage ... Leads statistical programming indication/disease area level strategies * Sets tasks and ...
Director, Statistical Programming
$242K - $293K/yr
In this role, Cluster Head, is responsible for managing employees: set objectives, manage ... Leads statistical programming indication/disease area level strategies * Sets tasks and ...
Director, Statistical Programming
$242K - $293K/yr
In this role, Cluster Head, is responsible for managing employees: set objectives, manage ... Leads statistical programming indication/disease area level strategies Sets tasks and ...
Director, Statistical Programming
$242K - $293K/yr
In this role, Cluster Head, is responsible for managing employees: set objectives, manage ... Leads statistical programming indication/disease area level strategies Sets tasks and ...
Lead and manage a statistical programming group, driving timely, high-quality deliverables across internal and outsourced work * Shape and implement programming standards, applications, processes ...
Lead and manage a statistical programming group, driving timely, high-quality deliverables across internal and outsourced work * Shape and implement programming standards, applications, processes ...
Sr. Statistical Programmer
Princeton, NJ · On-site
$75 - $80/hr
Study Programming and Deliverables * Independently manage and support multiple global clinical studies with minimal supervision. * Lead statistical programming activities for clinical trials ...
Sr. Statistical Programmer
Princeton, NJ · On-site
$75 - $80/hr
Study Programming and Deliverables * Independently manage and support multiple global clinical studies with minimal supervision. * Lead statistical programming activities for clinical trials ...
... a Statistical Analysis Plan, clinical pharmacology report requirement and programming ... Create, manage and maintain the programming specifications for the analysis datasets utilizing ...
... a Statistical Analysis Plan, clinical pharmacology report requirement and programming ... Create, manage and maintain the programming specifications for the analysis datasets utilizing ...
Interact with Global Clinical Operations, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze ...
New
Interact with Global Clinical Operations, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze ...
New
In this role, you will provide programming leadership and support for processing clinical trial ... Please speak with your recruiter and hiring manager for more information about onsite expectations ...
In this role, you will provide programming leadership and support for processing clinical trial ... Please speak with your recruiter and hiring manager for more information about onsite expectations ...
In this role, you will provide programming leadership and support for processing clinical trial ... Please speak with your recruiter and hiring manager for more information about onsite expectations ...
In this role, you will provide programming leadership and support for processing clinical trial ... Please speak with your recruiter and hiring manager for more information about onsite expectations ...
We are seeking a Manager to join our Biostatistics Hematology team. This position is for a ... Collaborating with Statistical Programming on the programming of tables, figures and listings to ...
We are seeking a Manager to join our Biostatistics Hematology team. This position is for a ... Collaborating with Statistical Programming on the programming of tables, figures and listings to ...
Sr. Principal Statistician, Biostatistics
Philadelphia, PA · On-site
$87K - $108K/yr
... management, and clinical operations. The Principal Statistician will oversee work done by ... Work closely with statistical programming colleagues. * Monitor CRO guidelines and standards to ...
Sr. Principal Statistician, Biostatistics
Philadelphia, PA · On-site
$87K - $108K/yr
... management, and clinical operations. The Principal Statistician will oversee work done by ... Work closely with statistical programming colleagues. * Monitor CRO guidelines and standards to ...
Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing Management & Operations etc. Who is proficient in Customer-level data analysis. Qualifications Who ...
Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing Management & Operations etc. Who is proficient in Customer-level data analysis. Qualifications Who ...
Sr. Principal Statistician, Biostatistics
Philadelphia, PA · On-site +1
$87K - $108K/yr
... management, and clinical operations. The Principal Statistician will oversee work done by ... Work closely with statistical programming colleagues. * Monitor CRO guidelines and standards to ...
Sr. Principal Statistician, Biostatistics
Philadelphia, PA · On-site +1
$87K - $108K/yr
... management, and clinical operations. The Principal Statistician will oversee work done by ... Work closely with statistical programming colleagues. * Monitor CRO guidelines and standards to ...
Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing Management & Operations etc. Who is proficient in Customer-level data analysis. Qualifications Who ...
Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing Management & Operations etc. Who is proficient in Customer-level data analysis. Qualifications Who ...
Senior Principal Statistician
$87K - $108K/yr
The Senior Principal Statistician will manage work done by statistics and programming external vendors. Essential Functions * Participate in department and cross-functional meetings to optimize ...
Senior Principal Statistician
$87K - $108K/yr
The Senior Principal Statistician will manage work done by statistics and programming external vendors. Essential Functions * Participate in department and cross-functional meetings to optimize ...
The Associate Director will manage work done by statistics and programming external vendors. Oversees professional development of any direct reports. Essential Functions * Participate in or lead ...
New
The Associate Director will manage work done by statistics and programming external vendors. Oversees professional development of any direct reports. Essential Functions * Participate in or lead ...
New
Manager Statistical Programming information
See Lambertville, NJ salary details
$82.9K - $97.6K
3% of jobs
$97.6K - $112.3K
10% of jobs
$122.2K is the 25th percentile. Wages below this are outliers.
$112.3K - $126.9K
18% of jobs
The median wage is $141.6K / yr.
$126.9K - $141.6K
19% of jobs
$154.4K is the 75th percentile. Wages above this are outliers.
$141.6K - $156.3K
29% of jobs
$156.3K - $171K
10% of jobs
$171K - $185.6K
12% of jobs
$185.6K - $200.3K
0% of jobs
$200.3K - $215K
0% of jobs
$215K - $229.7K
0% of jobs
$229.7K - $244.4K
0% of jobs
$82.9K
$144.5K
$244.3K
How much do manager statistical programming jobs pay per year?
What is a manager statistical programming?
A Manager Statistical Programming oversees a team of statistical programmers who support clinical trials and research by developing, validating, and maintaining statistical programs. They ensure compliance with regulatory requirements, manage project timelines, and collaborate with statisticians, data managers, and other stakeholders. This role requires strong programming skills in SAS or other statistical software, leadership abilities, and expertise in clinical data standards such as CDISC.
What are the typical daily responsibilities of a manager statistical programming?
As a Manager Statistical Programming, your daily responsibilities usually include overseeing a team of statistical programmers, coordinating the development and validation of statistical programs for clinical trial data analysis, and ensuring deliverables meet regulatory and company quality standards. You will often interact with biostatisticians, data managers, and clinical teams to align programming outputs with study goals. Additionally, you may review project timelines, allocate resources, mentor junior programmers, and contribute to process improvement initiatives. This multifaceted role requires balancing technical oversight with leadership and interdepartmental communication.
What are the key skills and qualifications needed to thrive in the manager statistical programming position, and why are they important?
To excel as a Manager Statistical Programming, you need a solid background in statistics, programming (such as SAS, R, or Python), and experience with clinical trial data management, often supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory guidelines (e.g., FDA, ICH), data standards such as CDISC, and certifications in relevant programming languages or clinical data processes are highly beneficial. Strong leadership, project management, and effective communication skills are essential for guiding teams and collaborating with cross-functional departments. These skills enable the manager to deliver high-quality statistical programming deliverables, ensure regulatory compliance, and drive team performance in a deadline-driven environment.
What cities near Lambertville, NJ are hiring for Manager Statistical Programming jobs?
Cities near Lambertville, NJ with the most Manager Statistical Programming job openings:

Manager Statistical Programming
Warren, NJ • On-site
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 9 days ago
Regeneron rating
8.6
Based on 45 frontline employees who took The Breakroom Quiz
Job description
Build our future together:
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.
This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where:
- Location: Warren, NJ or Cambridge, MA
- Work model/flexibility: Onsite
Discover your role:
- Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables
- Lead the development and quality control of tables, listings, and graphs in support of analysis requirements
- Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests
- Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch
- Partner with management to determine resource requirements for your therapeutic area or department
- Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles
- Provide feedback to management on team members' contributions to support performance evaluations and goal-setting
- Advise direct reports on procedures for data, records, and information retention
This role might be for you if you:
- Enjoy working with minimal supervision and taking ownership of complex deliverables
- Communicate clearly with cross-functional, multidisciplinary teams
- Think analytically and stay organized when managing multiple priorities and timelines
- Take initiative in developing deep expertise within a specialized area
- Bring a collaborative mindset to hiring, feedback, and team development
- Adapt easily to shifting priorities, including last-minute requests from senior leadership
- Approach quality and documentation with rigor in a regulated environment
This role requires:
- Master's degree with 8-10 years of relevant work experience (or a Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of relevant programming experience, including some project and people management experience)
- Proven experience leading programming deliverables within a clinical study team
- Experience providing input on hiring, feedback, and performance evaluation
- Strong organizational and documentation skills within a regulated environment
Nice to haves:
- SAS Certification
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$128,600.00 - $210,000.00What Regeneron employees say
Pay
Benefits
Hours and flexibility
Workplace
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About Regeneron
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
5,001 - 10,000 Employees
Headquarters location
Tarrytown, NY, US
Year founded
1988