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Manager Statistical Programming Jobs in Coatesville, PA

Ra

Marketing Analytics Manager

Wilmington, DE

Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing Management & Operations etc. Who is proficient in Customer-level data analysis. Qualifications Who ...

Ra

Marketing Analytics Senior Manager

Wilmington, DE

Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing Management & Operations etc. Who is proficient in Customer-level data analysis. Qualifications Who ...

TechData Service Company LLC

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Remote Statistician-Real World Evidence (RWE)

King Of Prussia, PA · Remote

$100K - $160K/yr

... statistical programming languages/software such as SAS and/or R · Able to work in a virtual ... management skills with a focus on results for timely and accurate completion of competing ...

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All JobsStatistical Programming JobsManager Statistical Programming JobsManager Statistical Programming Jobs in Coatesville, PA

Manager Statistical Programming information

See Coatesville, PA salary details

$82.8K

$144.4K

$244K

How much do manager statistical programming jobs pay per year?

As of Sep 4, 2026, the average yearly pay for manager statistical programming in Coatesville, PA is $144,358.00, according to ZipRecruiter salary data. Most workers in this role earn between $122,500.00 and $156,800.00 per year, depending on experience, location, and employer.

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.

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Manager Statistical Programming jobs near you
Infographic showing various Manager Statistical Programming job openings in Coatesville, PA as of August 2026, with employment types broken down into 79% Full Time, 20% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $144,358 per year, or $69.4 per hour.

Senior Director, Statistical Programming

Aclaris Therapeutics, Inc.

Wayne, PA • On-site, Remote

Full-time

Posted 3 days ago

New

Key responsibilities

  • Lead the statistical programming team by creating workflows, standards, and SOPs.

  • Manage programming timelines and oversee the work of CROs and external vendors.

  • Review and check SAS programs to ensure they meet study requirements and provide support for data review and reporting activities.

Job description

Description
Position Summary:
The Senior Director, Statistical Programming leads our data and analytics efforts. In this role, you will build and manage the statistical programming strategies, SAS frameworks, and team standards needed to support Aclaris's clinical programs. You will manage programmers and CROs, oversee programming activities and provide timely support to the cross-functional teams on statistical programming matters according to the project strategies and requests. This role will be hands-on initially with the opportunity to build the function as our clinical programs advance.
Essential Duties and Responsibilities:
  • Lead the statistical programming team by creating clear workflows, standards, and standard operating procedures (SOPs).
  • Manage programming timelines for clinical studies and oversee the work of CROs and external vendors.
  • Partner with Biostatistics, Data Management, Clinical Operations, Regulatory, Pharmacovigilance, and other functions to deliver high-quality data deliverables in timely fashion.
  • Help develop new data review tools and reporting applications alongside the Biostatistics team.
  • Review and check SAS programs created by CROs to ensure they meet standard (e.g., SDTM, ADaM) and custom (e.g., non-standard datasets and TFLs) study requirements.
  • Develop SAS infrastructure and programming processes to make routine reporting and ad hoc data requests more efficient.
  • Review and provide expert feedback on study documents like SAPs, DMPs, CRFs, data and TFL programming specifications.
  • Hire, train, and mentor a team of programmers to support our growing clinical trials.
  • Run ad hoc data analyses as needed to support business decisions.

Additional Responsibilities:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.
Requirements
Required Education and Experience:
  • Master's Degree in Statistics, Biostatistics, Mathematics, or a related field.
  • At least 10 years of clinical trial programming experience in the pharma or biotech industry.

Required Knowledge, Skills, Abilities & Behaviors:
  • Strong SAS programming skills, with some experience using other tools like R.
  • Deep understanding of CDISC standards, including SDTM, ADaM, and controlled terminologies.
  • Great organizational skills and the ability to balance multiple tasks in a fast-paced environment.
  • Strong communication skills and the ability to explain technical data concepts to other teams.
  • Proven experience managing CROs and external data vendors.
  • A supportive leader who values a collaborative and psychologically safe team environment.
  • Good working knowledge of FDA, EMA, and ICH regulatory guidelines.
  • Comfortable working and leading in a fully remote, virtual environment.
  • Willing and able to travel for business as needed.

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