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Manager Statistical Programming Jobs in Pennsylvania

Additionally, experience in managing ADaM standards would be a valuable plus. What You Will Do: Your experience in statistical programming will be key in delivering high-quality outcomes and ...

Additionally, experience in managing ADaM standards would be a valuable plus. What You Will Do: Your experience in statistical programming will be key in delivering high-quality outcomes and ...

Able to work independently in a remote environment and manage timelines effectively. Preferred Qualifications: * Experience with R for data analysis, programming, or statistical workflows is highly ...

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Manager Statistical Programming information

See Pennsylvania salary details

$84.7K

$147.6K

$249.6K

How much do manager statistical programming jobs pay per year?

As of Jun 14, 2026, the average yearly pay for manager statistical programming in Pennsylvania is $147,645.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,300.00 and $160,400.00 per year, depending on experience, location, and employer.

What is a Manager Statistical Programming job?

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 are the most commonly searched types of Statistical Programming jobs in Pennsylvania? The most popular types of Statistical Programming jobs in Pennsylvania are:
What are popular job titles related to Manager Statistical Programming jobs in Pennsylvania? For Manager Statistical Programming jobs in Pennsylvania, the most frequently searched job titles are:
What job categories do people searching Manager Statistical Programming jobs in Pennsylvania look for? The top searched job categories for Manager Statistical Programming jobs in Pennsylvania are:
What cities in Pennsylvania are hiring for Manager Statistical Programming jobs? Cities in Pennsylvania with the most Manager Statistical Programming job openings:
Executive Director, Statistical Programming

Executive Director, Statistical Programming

Merck & Co., Inc.

North Wales, PA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago


Merck rating

7.8

Company rating: 7.8 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

41st of 71 rated pharmaceutical


Job description

Job Description
Reporting to the Head of Statistical Programming (SP), the Executive Director leads a team of statistical programmers and analysts supporting foundational analysis and reporting tools, including standard code libraries, platforms, processes, training, and the generation and management of clinical schedules for our company's clinical trial pipeline.
As a key member of the Statistical Programming Leadership Team, this role serves as a strategic and influential leader, models effective people management, and establishes the team's strategic and operational objectives. The Executive Director also fosters productive collaboration with stakeholders across Biostatistics and Research Decision Sciences, Data Management, IT, Quality, Clinical, and Regulatory Affairs.
Primary Responsibilities:
  • Leads the delivery of analysis and reporting tools, processes, platforms, and training for Biostatistics and Research Decision Sciences (BARDS) staff supporting all clinical trial phases and therapeutic areas, with a focus on regulatory compliance, quality, and efficiency. Partners with Statistics and Statistical Programming leaders, aligns work to the company scorecard, and collaborates with stakeholders and functional service partners.
  • Manages managers and builds high-performing teams by recruiting, hiring, developing, and evaluating staff; implementing talent management strategies; coaching and mentoring employees; and contributing to succession and workforce planning.
  • Contributes to the broader vision and strategy of the Statistical Programming organization as a member of the leadership team, challenging the status quo, driving innovation, and applying strong business acumen.
  • Maintains current knowledge of regulatory guidance and submission standards.
  • Manages team headcount and budget, and collaborates with vendors and partnership management to maintain flexible and cost-effective programming resources.
  • Leads departmental and strategic initiatives, developing and executing long-term and annual operating objectives for assigned areas within Statistical Programming.
  • Represents the organization externally by participating in industry initiatives and engaging with statistical programming and regulatory thought leaders, including contributing to, organizing, or chairing sessions at professional meetings.

Education and Minimum Requirement:
  • Master's degree in statistics, computer science or closely related field is preferred. The position requires at least 12 years of experience in statistical programming, statistics, or closely related activity in a pharmaceutical development environment and at least 5 years of management experience at the Director level.

Required Skills and Experience:
  • Deep knowledge of clinical trial operations, statistical analysis and reporting processes, regulatory and industry compliance standards, and the software development lifecycle.
  • Extensive experience leading or managing statistical programming teams responsible for analysis and reporting deliverables, including recruiting, hiring, performance management, and employee development.
  • Strong ability to negotiate and collaborate across business domains and cultures, while managing a broad portfolio of work.
  • Excellent oral and written communication skills, with experience collaborating in a global environment across functions such as statistics, IT, data management, quality, clinical and regulatory affairs.
  • Strong interpersonal and project management skills, with the ability to prioritize, align stakeholders, and lead across boundaries.
  • Experience managing complex, cross-functional programs and ensuring strategic alignment, consistency, and compliance.
  • Experience working with external vendors for resources and software.
  • Ability to thrive in a dynamic, fast-paced environment, make sound decisions quickly, and navigate ambiguity effectively.

Preferred Skills and Experience:
  • Strong track record of setting strategy for efficient analysis and reporting deliverables and tools.
  • Experience leading teams through technological change, evolving standards, shifting priorities, and complex challenges.
  • Ability to implement practical programming solutions with urgency and impact in ambiguous situations.
  • Experience managing other managers.

Required Skills:
Clinical Trials Operations, Cross-Functional Leadership, Executive Leadership, Pharmaceutical Industry, Program Management, Project Management, Regulatory Compliance, Reporting Processes, Software Development Life Cycle (SDLC), Statistical Analysis, Statistical Programming, Statistics, Vendor Management
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
The salary range for this role is
$231,900.00 - $365,000.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
06/13/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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