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Merck Biostatistics Jobs (NOW HIRING)

Merck & Co.

$47K - $64K/yr

Adaptability, Adaptability, Analytical Chemistry, Biomarker Identification, Biostatistics, Cell ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

Merck & Co.

Education Doctoral or Master's degree in Health Economics, Economics, Biostatistics, Actuarial ... 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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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.
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Merck Biostatistics jobs near you
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.
Senior Scientist, Statistical Programming

Senior Scientist, Statistical Programming

Merck & Co.

North Wales, PA

Full-time

Posted 3 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 DescriptionResponsibilities:Support statistical programming activities for clinical trial data analysis.Develop SAS programs to create and validate analysis datasets (ADaM) and summaries (TFLs) in support of Clinical Study Reports and regulatory submissions (FDA, EMA, etc.).Collaborate with biostatisticians, project leads, and other stakeholders in ensuring project plans are executed efficiently with timely and high-quality deliverables.Develop effective study and report programming and validation utilizing global CDISC, ICH, and Therapeutic Areas standards and following departmental SOPs and good programming practices.Maintain and manage a project plan including resource forecasting. Coordinate activities of a global programming team. Participate in departmental strategic initiative teams.Requirements:Master's degree or equivalent in Computer Science, Statistics, Applied Mathematics, Biomedical Engineering, or a closely related field and 3 years of experience in the position offered or a related role; OR a Bachelor's degree or equivalent in Computer Science, Statistics, Applied Mathematics, Biomedical Engineering, or a closely related field and 5 years of experience in the position offered or a related role.Must have 3 years of experience with all the following:Developing analysis and reporting deliverables for Phase 2 and 3 clinical trials, including creation of analysis datasets, tables, graphics, and listings, for planned and unplanned analyses.SAS programming in a clinical trial environment including data step and procedures, macros, graphics, ODS.Interpreting and executing on clinical trial statistical analysis plans.Utilizing CDISC standards to create ADaM and SDTM datasets.Designing and developing complex programming algorithms.Ensuring process compliance and deliverable quality.Required Skills:-Preferred Skills:Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: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.

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:No relocationVISA Sponsorship:No Travel Requirements: No Travel RequiredFlexible Work Arrangements:Not ApplicableShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:08/19/2026 *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:R395927 Salary: . Date posted: 06/06/2026

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