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Merck Biostatistics Jobs (NOW HIRING)

... Biostatistics, Biophysics, Genetics/Genomics, or a STEM related discipline, preferably with 3+ ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

... biostatistics, drug metabolism, modeling and simulation, regulatory affairs, and global clinical ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

PKPD, pharmacometrics, mathematics, statistics/ biostatistics, or chemical/biomedical engineering ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

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Merck Biostatistics information

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$57

$106

How much do merck biostatistics jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for merck biostatistics in the United States is $57.55, according to ZipRecruiter salary data. Most workers in this role earn between $40.62 and $64.42 per hour, depending on experience, location, and employer.

What is the difference between Merck Biostatistics vs Merck Data Analysis?

AspectMerck BiostatisticsMerck Data Analysis
Required CredentialsBiostatistics degree, statistical certificationsData analysis degree, data management certifications
Work EnvironmentClinical trials, research teamsData management, reporting teams
Employer & Industry UsagePharmaceutical research, clinical developmentPharmaceutical industry, data-driven decision making

Merck Biostatistics focuses on designing and analyzing clinical trial data, requiring expertise in biostatistics and statistical methods. Merck Data Analysis involves managing and interpreting large datasets for various business insights, emphasizing data management skills. While both roles support Merck's research and development, biostatistics is more specialized in clinical trial analysis, whereas data analysis covers broader data-driven tasks within the company.

What do biostatisticians at Merck do?

Biostatisticians at Merck play a crucial role in designing, analyzing, and interpreting data from clinical trials and other research studies. They collaborate with scientists, clinicians, and regulatory teams to ensure that statistical methods are appropriately applied, helping to make informed decisions about drug efficacy and safety. Their work supports the development of new medicines by providing accurate, reliable data analyses that comply with regulatory standards. They also contribute to study protocol development, data management strategies, and regulatory submissions.

How do biostatisticians at Merck typically collaborate with clinical research teams during a drug development project?

At Merck, biostatisticians work closely with clinical research teams throughout the drug development process. They are involved from the study design phase, helping to ensure robust statistical methodologies, and continue to provide ongoing data analysis support as trials progress. Regular cross-functional meetings facilitate collaboration with clinical scientists, data managers, and regulatory affairs professionals, ensuring that statistical insights are effectively integrated into decision-making. This collaborative environment helps biostatisticians contribute significantly to the interpretation of clinical trial results and the preparation of regulatory submissions.

How much does Merck Senior Scientist Statistical Programmers make?

Senior Statistical Programmers at Merck typically earn between $90,000 and $130,000 annually, depending on experience, location, and education. These roles often require proficiency in statistical software such as SAS or R and may include additional benefits like bonuses and health insurance.

What are the key skills and qualifications needed to thrive as a Biostatistician at Merck, and why are they important?

To thrive as a Biostatistician at Merck, you need a strong background in statistics or biostatistics, typically with an advanced degree (MS or PhD), and experience in clinical trial design and data analysis. Proficiency in statistical software such as SAS, R, or Python, and familiarity with regulatory guidelines (e.g., FDA, ICH) are essential. Excellent communication, problem-solving abilities, and collaboration skills set candidates apart in cross-functional project teams. These competencies ensure robust statistical analyses that support successful drug development and regulatory submissions.
What cities are hiring for Merck Biostatistics jobs? Cities with the most Merck Biostatistics job openings:
What states have the most Merck Biostatistics jobs? States with the most job openings for Merck Biostatistics jobs include:
What job categories do people searching Merck Biostatistics jobs look for? The top searched job categories for Merck Biostatistics jobs are:
Infographic showing various Merck Biostatistics job openings in the United States as of June 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $119,702 per year, or $57.5 per hour.
Assoc Principal Scientist Statistical Programming, Late-Stage (Hybrid)

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

Merck & Co.

Rahway, NJ

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 28 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.This position supports statistical programming activities for multiple and/or large/complex 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 databases 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.Key areas of focus include: The assurance of deliverable quality and process compliance.Effective deliverable development utilizing global and TA standards that optimize analysis and reporting and promote a strategic knowledge-base data model.Maintaining and managing a project plan including resource forecasting. -Coordinating the activities of a global programming team that includes outsource provider staff.Membership on departmental strategic initiative project teams such as new statistical computing platform evaluation and development.

Education and Minimum Requirement: BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering-or related field plus 9 years or more SAS programming experience in a clinical trial environment. ORMS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or-related field plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Experience leading large and/or complex statistical programming projects that include coordinating the activities of a programming team.Broad knowledge and significant experience in developing analysis and reporting statistical programming deliverables (datasets, statistical analyses, report tables, and graphics) using global and TA standards and according to quality, compliance and timeliness requirements.-Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise.

Familiarity with statistical analysis methods and clinical data management concepts.US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development of electronic submission deliverables.Strong project management skills; A program leader; Determines appropriate programming methodology, assures programming consistency across protocols and projects, completes programming tasks, and directs the program development effort of other programmers; an experienced programming mentor; ability to engage key stakeholders.Ability to comprehend statistical analysis plans which may describe statistical methodology to be programmed; Understanding of statistical terminology and concepts Designs and develops complex programming algorithms.Excellent communication and negotiation skills with a demonstrated history of teamwork and collaboration; deals well with change and seamlessly assimilates to new projects and stakeholders.Strategic 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-practices.Experience in CDISC and ADaM standards.Demonstrated success in the assurance of deliverable quality and process compliance.Ability to anticipate stakeholder and regulatory requirements. Preferred Experience and Skills: Strong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC).Ability and interest to work across cultures and geographies.Experience providing technical and/or programming guidance and mentoring to colleagues.Ability 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 societies.Experience in process improvement.BARDS2020eligibleforERPSPjobsVETJOBSEBRGRequired Skills: Data Management, Data Modeling, Numerical Analysis, Stakeholder Relationship Management, Waterfall ModelPreferred 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 $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: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:R398456 Salary: . Date posted: 05/28/2026


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