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Associate Director Statistical Programming Jobs in New York

Learn more at Associate Director, Market Access Analytics and Real World Evidence (MAA & RWE ... Provide expert guidance on statistical methodologies and programming approaches to address key ...

Associate Director, Statistics

Florham Park, NJ · On-site

$61K - $62K/yr

Direct the development of scientific protocols, ensuring they are scientifically sound, aligned ... Statistical Programming and other stakeholders to evaluate existing databases, both clinical ...

New

Direct the development of scientific protocols, ensuring they are scientifically sound, aligned ... Statistical Programming and other stakeholders to evaluate existing databases, both clinical ...

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Associate Director Statistical Programming information

See New York salary details

$167.9K

$306.5K

$376.3K

How much do associate director statistical programming jobs pay per year?

As of Sep 14, 2026, the average yearly pay for associate director statistical programming in New York is $306,491.00, according to ZipRecruiter salary data. Most workers in this role earn between $285,000.00 and $352,800.00 per year, depending on experience, location, and employer.

What does an associate director statistical programming do?

An Associate Director of Statistical Programming leads teams responsible for the design, development, and validation of statistical programs used in the analysis of clinical trial data. They oversee the creation of datasets, tables, listings, and figures that support regulatory submissions and scientific publications. In addition to technical expertise, this role involves managing timelines, ensuring compliance with regulatory standards, and collaborating with cross-functional teams such as biostatistics, data management, and clinical operations.

What are the key skills and qualifications needed to thrive as an associate director statistical programming?

To thrive as an Associate Director Statistical Programming, you need expertise in statistical programming, clinical trial data standards, and a degree in statistics, mathematics, or a related field, often with several years of experience in the pharmaceutical or biotechnology industry. Proficiency in programming languages such as SAS and R, knowledge of CDISC standards (SDTM, ADaM), and familiarity with regulatory submission requirements are typically required. Strong leadership, project management, and communication skills are vital for guiding teams and collaborating with cross-functional partners. These skills and qualities ensure the delivery of high-quality, compliant statistical outputs that support clinical development and regulatory approval.

How does an associate director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech setting?

As an Associate Director of Statistical Programming, you will work closely with biostatisticians, clinical data managers, and regulatory affairs professionals to ensure that statistical analyses and data outputs meet project and regulatory requirements. You’ll often lead programming teams, coordinate timelines, and help translate statistical analysis plans into executable code. Regular meetings and clear communication are key, as you’ll be expected to provide technical guidance and ensure data integrity across multiple studies or programs. This role often requires balancing hands-on programming with strategic leadership and mentorship responsibilities.

What is the difference between Associate Director Statistical Programming vs Statistical Programmer?

AspectAssociate Director Statistical ProgrammingStatistical Programmer
Required CredentialsBachelor's or Master's in Biostatistics, Statistics, or related field; experience in clinical trial programmingBachelor's or Master's in similar fields; entry to mid-level experience
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms programming tasks, supports project teams, executes statistical analyses
Employer & Industry UsagePharmaceutical and biotech companies, clinical research organizationsPharmaceutical companies, CROs, biotech firms

The Associate Director Statistical Programming typically oversees programming teams and manages project deliverables, requiring leadership skills and extensive experience. In contrast, the Statistical Programmer focuses on executing programming tasks under supervision. Both roles are essential in clinical research, but the Associate Director holds more managerial responsibilities and strategic oversight.

What are popular job titles related to Associate Director Statistical Programming jobs in New York?

For Associate Director Statistical Programming jobs in New York, the most frequently searched job titles are:

What job categories do people searching Associate Director Statistical Programming jobs in New York look for?

The top searched job categories for Associate Director Statistical Programming jobs in New York are:

What cities in New York are hiring for Associate Director Statistical Programming jobs?

Cities in New York with the most Associate Director Statistical Programming job openings:

Infographic showing various Associate Director Statistical Programming job openings in New York as of August 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Hybrid job distribution, with an average salary of $306,491 per year, or $147.4 per hour.

Assoc Principal Scientist Statistical Programming, Late-Stage (Non-Oncology) (Hybrid)

Rahway, NJ • On-site

Merck & Co.
Pharmaceutical Product Wholesalers • 10K+ employees

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

New


Merck rating

7.9

Company rating: 7.9 out of 10

Based on 52 frontline employees who took The Breakroom Quiz


Job description

Job DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.This position leads statistical programming activities for multiple and/or late-stage drug/vaccine clinical-development projects. Accountability predominantly includes the development and execution of statistical-analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures), the span of-which range from individual clinical trials to world-wide regulatory application submissions and post marketing-support.-The incumbent is responsible for the design and maintenance of statistical datasets that support multiple-stakeholder groups which include clinical development, outcomes research and safety evaluation.-The position is a key collaborator with statistics and other project stakeholders in ensuring that project plans are-executed efficiently with timely and high-quality deliverables.-For assigned projects the position serves as the statistical programming point of contact and knowledge holder-through the entire product lifecycle.-Primary Activities: Effective analysis and report programming development and validation utilizing global and TA standards and-Following departmental SOPs and good programming practicesMaintain and manage a project plan including resource forecasting-Coordinate the activities of a global programming team that includes outsource provider staffMembership on departmental strategic initiative teamsEducation and Minimum Requirement: BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 7 years SAS programming experience in a clinical trial environmentDepartment Required Skills and Experience: Excellent interpersonal skills and ability to negotiate and collaborate effectivelyExcellent written, oral, and presentation skillsBroad knowledge and significant experience in developing analysis and reporting deliverables for R&D projects-(data, analyses, tables, graphics, listings)Strong project management skills; leadership at a program level; determines approach and ensures-consistency and directs development of others when opportunities arise; ability to engage key stakeholders Position Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertiseExperience leading large and/or complex statistical programming projects that include coordinating the activities of a programming teamUS and/or worldwide drug or vaccine regulatory application submission experience at the leadership level-including the development of electronic submission deliverablesDesigns and develops complex programming algorithmsAbility to comprehend analysis plans which may describe methodology to be programmed; an understanding-of statistical terminology and conceptsFamiliarity with clinical data management conceptsExperience in CDISC and ADaM standardsDemonstrated success in the assurance of deliverable quality and process complianceStrategic thinking - ability to turn strategy into tactical activities; design of statistical databases with the end in-mind that optimize analysis and reporting and leverage departmental standards and industry best-practicesAbility to anticipate stakeholder requirements** Preferred Skills and Experience: Strong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)Experience with GenAI tools (e.g., Python, R, R Shiny, Claude, etc.)Experience providing technical and/or programming guidance and mentoring to colleaguesAbility and interest to work across cultures and geographiesAbility to complete statistical programming deliverables through the use of global outsource partner programming staff-Experience developing and managing a project plan using Microsoft Project or similar package-Active in professional societiesExperience in process improvementBARDS2020eligibleforERPSPjobsVETJOBSEBRGRequired Skills: CDISC ADaM, Clinical Data Interchange Standards Consortium (CDISC) Standards, Project Management, Regulatory Submissions, Stakeholder Relationship Management, Statistical Analysis Systems (SAS) ProgrammingPreferred Skills: Generative AI, Python (Programming Language), R ProgrammingCurrent 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 $142,400.00 - $224,100.00This 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: RegularRelocation:DomesticVISA Sponsorship:Yes Travel Requirements: 10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:09/25/2026 *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. Requisition ID:R416557 Salary: . Date posted: 09/12/2026

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