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Per Diem Senior Statistical Programmer Jobs (NOW HIRING)

Role Summary The Sr Manager, Statistical Programming is responsible for the development of ... Some domestic and international travel required (2-3 times per year) * On-site in Boston ...

The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This position performs statistical programming for ...

Statistical Programmer II

Newton, MA · On-site

$115K - $132K/yr

Job Location : 275 Grove Street, Suite 101C, Newton, MA 02466 and position may telecommute from anywhere in the United States 5 days per week. Job Title : Statistical Programmer II Duties: Parexel ...

Statistical Programmer II

Newton, MA · On-site

$115K - $132K/yr

Job Location: 275 Grove Street, Suite 101C, Newton, MA 02466 and position may telecommute from anywhere in the United States 5 days per week. Job Title: Statistical Programmer II Duties: Parexel ...

... Senior Management levels * Creates all files, documents, and analyses necessary to support an ... to two days per week; or select 3. On-Site : work five days per week on-site with ad hoc ...

Statistical Programmer II

Newton, MA · On-site +1

$115K - $132K/yr

Job Location: 275 Grove Street, Suite 101C, Newton, MA 02466 and position may telecommute from anywhere in the United States 5 days per week. Job Title: Statistical Programmer II Duties: Parexel ...

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Per Diem Senior Statistical Programmer information

See salary details

$82.5K

$128.3K

$167.5K

How much do per diem senior statistical programmer jobs pay per year?

As of Jun 8, 2026, the average yearly pay for per diem senior statistical programmer in the United States is $128,293.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,000.00 and $148,000.00 per year, depending on experience, location, and employer.

What is the difference between Per Diem Senior Statistical Programmer vs Statistical Programmer?

AspectPer Diem Senior Statistical ProgrammerStatistical Programmer
CredentialsTypically requires a degree in biostatistics, statistics, or related field; experience often preferredSame as senior role, usually a degree in a relevant field; less experience required
Work EnvironmentContract-based, flexible hours, often remote or onsite at clinical research organizationsFull-time, permanent position, may be onsite or remote in pharmaceutical or biotech companies
Employer & Industry UsageUsed by CROs, pharma companies for short-term projectsCommon in pharmaceutical, biotech, and CROs for ongoing roles

The main difference is that a Per Diem Senior Statistical Programmer works on a temporary, contract basis with flexible hours, often remotely, while a Statistical Programmer typically holds a full-time, permanent position. Both roles require similar credentials, but the employment type and work arrangement distinguish them.

What is a Per Diem Senior Statistical Programmer?

A Per Diem Senior Statistical Programmer is a highly experienced professional who works on a temporary or as-needed basis, primarily in clinical research or pharmaceutical settings. Their main responsibilities include programming statistical analyses, generating reports, and ensuring data accuracy using statistical software such as SAS. They often collaborate with biostatisticians, data managers, and clinical teams to support clinical trial data analysis and regulatory submissions. The 'per diem' status means they are paid daily or hourly and their work schedule is flexible, depending on project demands.

How does the flexibility of a per diem Senior Statistical Programmer position impact collaboration with study teams?

As a per diem Senior Statistical Programmer, your flexible schedule often means collaborating remotely or during specific project phases. While this flexibility is a major benefit, it requires strong communication skills and proactive coordination to stay aligned with full-time team members, statisticians, and data managers. You’ll likely participate in regular virtual meetings, update project documentation, and use collaborative tools to ensure deadlines and quality standards are met. Balancing autonomy with timely responsiveness is key to success in this role.

What are the key skills and qualifications needed to thrive as a Per Diem Senior Statistical Programmer, and why are they important?

To thrive as a Per Diem Senior Statistical Programmer, you need advanced proficiency in statistical programming languages like SAS or R, a strong understanding of clinical trial data, and a relevant degree in statistics, mathematics, or a related field. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and familiarity with data management systems are typically required. Exceptional problem-solving, attention to detail, and effective communication skills help distinguish top performers in this role. These skills ensure the accuracy and integrity of clinical data analysis, supporting regulatory compliance and successful trial outcomes.
More about Per Diem Senior Statistical Programmer jobs
What are the most commonly searched types of Senior Statistical Programmer jobs? The most popular types of Senior Statistical Programmer jobs are:
What job categories do people searching Per Diem Senior Statistical Programmer jobs look for? The top searched job categories for Per Diem Senior Statistical Programmer jobs are:
Sr. Scientist, Stat. Programming - SDTM (Hybrid)

Sr. Scientist, Stat. Programming - SDTM (Hybrid)

Merck & Co.

North Wales, PA

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 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 DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our 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. Responsibilities :The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes submission data standards planning activities, coaching and consulting with project teams, outreach to external vendors and partners, and keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.The incumbent will be responsible for continuous improvement of our electronic submission process and providing tools and templates to support delivery focusing on traceability, quality assurance, data conformance and data fitness.

The position is a key collaborator with statistical programming, statistics, regulatory and other project stakeholders. Primary Activities :PreNDA and PreBLA meeting preparation, study data standards plan, preparing questions for FDA e-data mailboxes (CBER/CDER), attendance at meetings with regulatory agencies (FDA, EMA, PMDA),Guiding project teams preparing submission deliverables including use of Pinnacle 21 Enterprise,Up-versioning activities to specific versions of SDTMParticipation in industry teams and conferences on best practicesMembership on departmental strategic initiative project teams Education and Minimum Requirement :BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial environment Department Required Skills and Experience: Effective interpersonal skills and ability to negotiate and collaborate effectivelyEffective written, oral, and presentation skillsEffective knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings)A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholder Position Specific Required Skills and Experience: US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverablesExperience with submission standards CDISC (SDTM, ADaM), Define.XML, cSDRG, ADRGDemonstrated success in the assurance of deliverable quality and process compliance.Excels in technical writing, able to convert complex ideas and information into simple readable formSolid project management skillsFamiliarity with clinical data management conceptsStrategic thinking - ability to turn strategy into tactical activitiesAbility to anticipate stakeholder requirements** Preferred Skills and Experience: Hands-on experience with R and Python for data analysis and statistical modelingStrong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)Experience assuring consistency across protocols and projectsAbility and interest to work across cultures and geographiesAbility to complete statistical programming deliverables through the use of global outsource partner programming staffExperience developing and managing a project plan using Microsoft Project or similar packageActive in professional societiesExperience in process improvementeligibleforERPSPjobsBARDS2020VETJOBSEBRGRequired Skills: Clinical Trials, Computer Programming, Computer Science, Data Management, Data Modeling, Electronic Submissions, Microsoft Project, Numerical Analysis, Process Improvements, Project Management, Regulatory Compliance, SDTM Mapping, Stakeholder Relationship Management, Statistical Programming, Strategic Thinking, Study Data Tabulation Model (SDTM), Technical Writing, Waterfall ModelPreferred Skills: 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 $117,000.00 - $184,200.00This 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:06/11/2026 *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:R399775 Salary: . Date posted: 05/28/2026


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