S4 Analytics LLC is a fast growing IT and Clinical staffing company. Our direct clients include Johnson and Johnson, Shionogi and Omeros. Our key focus areas are Clinical SAS programmers and CDMs for Clinical Trails, Manual Testing, Test Automation, SDET, RPA, DevOps, JAVA, ETL& Reporting, Data Engineering and Visualization tools.

Industry: IT Services and IT Consulting
Company Size: 11-50 employees

S4 Analytics LLC

Savvy Admin PROD

**Job Title: ** Senior Biostatistician

**Location: ** NJ

**Experience:1 - 10 **+ Years

**Job Type: ** Contract / Full-Time

**Job Description: **

We are seeking an experienced Senior Biostatistician to join our Biostatistics and Statistical Modelling team. The candidate will be responsible for designing and analyzing clinical trials, supporting clinical development activities, and delivering statistical outputs for regulatory submissions. This role involves close collaboration with cross-functional teams and stakeholders.

**Roles & Responsibilities: **

- Lead statistical planning and analysis for Phase II–IV clinical trials

- Collaborate with stakeholders to define analysis strategies and ensure timely delivery

- Prepare submission-ready datasets including eCRT packages and Define-XML documentation

- Ensure compliance with regulatory and internal standards

- Support clinical development plans and reporting activities

- Mentor and guide junior statisticians and programmers

- Communicate findings and updates to stakeholders and leadership

**Required Skills: **

- Master’s or Ph.D. in Statistics, Biostatistics, or related field

- 1 - 5+ years of experience in clinical trial biostatistics

- Strong proficiency in SAS and/or R

- Experience with eCRT and Define-XML for regulatory submissions

- Good understanding of clinical trials and drug development processes

- Strong analytical and problem-solving skills

- Excellent communication and documentation skills

Apply / Refer:Abhi

Jr IT Recruiter | S4 Analytics

Phone: +1 (469)429-8068

Email: Abhi@s4analytix.com

Senior Biostatistician

Welcome to DataAnnotation! We pay smart folks to train AI. We offer a remote, flexible work model- you choose your own hours and get to work when you want, whenever you want. Apply now through our open Job Listings.

Industry: Software Development
Company Size: 5,001-10,000 employees

DataAnnotation

We are looking for a Biostatistician to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.

In this role you will need to hold an understanding of biology as well as an expert level of statistical reasoning. Other related fields include, but are not limited to: Applied Mathematics and/or Computer Science.

**Benefits**

- This is a full-time or part-time REMOTE position

- You’ll be able to choose which projects you want to work on

- You can work on your own schedule

- Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work

**Responsibilities**

- Give AI chatbots diverse and complex mathematics problems and evaluate their outputs

- Evaluate the quality produced by AI models for correctness and performance

**Qualifications**

- Fluency in English (native or bilingual level)

- Detail-oriented

- Proficient in probability, statistics, mathematics, biology, and inductive/deductive reasoning

- A current, in progress, or completed Masters and/or PhD is preferred but not required

**Notes**

Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Only applicants in the United States will be considered for this role. This is an independent contract position.

#bio

Biostatistician

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.  
 
We bring together a talented team of professionals, who work across more than 110 countries, with a deep understanding of patient and physician behaviors and market dynamics. 
Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. 
 
Syneos Health supports a diverse, equitable and inclusive culture that cares for colleagues, customers, patients, communities and the environment.

Industry: Biotechnology Research
Company Size: 10,001+ employees

Syneos Health

**Description**

Sr Biostatistician-Sr Data Scientist/Analyst (US and UK Only)

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

-  We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.

-  We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.

-  We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

**Job Responsibilities**

- Must be located in the United States or UK with no sponsorship needs to be considered for this position.

Core Function Description:

Lead development of analysis specifications, develop programs, and conduct analyses while providing technical guidance for Real World Data (RWD) research. Ensure quality standards and methodological rigor across projects through development of patient cohorts and validation of key variables.

Required Experience:

-  Leadership of RWD analysis strategy and execution

-  Lead development of technical specifications and study methodology

-  Statistical programing proficiency (R, SAS, SQL., Python)

-  Oversight of quality control processes

-  Cross-functional team collaboration

-  Management of project timelines and deliverables

-  Development of best practices and standards

-  Demonstrated ability to communicate complex analyses to non-technical stakeholders

-  Technical Expertise

- Proficiency in SAS or R & SQL is a must, expectation to be programming independently, creating packages, taking requirements, writing specifications, work with complex data structures and study design.

- Experience in more complex programming, such as propensity score analysis, lines of therapy, Sankey diagram, machine learning

- Experience with complex statistical programing, such as propensity score matching

- Experience applying machine learning methods (such as LASSO, DT, RF, and XGBoost) with RWD

-  Experience with OHDSI or DARWIN tool sets in RSubject Matter Expertise

- Understanding of epidemiology / outcomes research, experience with study design and execution, Biomarker/genomic data sources

- Experience with healthcare databases:

&#61607; Claims (examples include Optum, MarketScan, Pharmetrics+, HealthVerity, CPRD)

&#61607; Electronic Health Records (examples include IQVIA, Flatiron, Concert AI, TriNetX)

&#61607; Experience with OMOP CDM or similar common data model framework

- Knowledge of US/international data sources

- For clinical trial analysis specifically, experience with psychometric validation

-  Project Implementation capability (reviewing, contributing to technical review and suggesting edits, executing) in the following are expected

- Statistical analysis plan development

- Protocol / manuscript development

- Study design and execution

- Cross-functional team collaboration

- Being able to track and update work in a software (Jira or ADO)

**Minimum Qualifications**

-  Master’s degree is Biostatistics, Epidemiology, Data Science, Bioinformatics, or related field with 5-8 years of relevant post-graduation experience or PhD with 3+ years post-graduation experience

17

-  Advanced expertise in statistical programming and observational research methods

-  Comprehensive experience with healthcare data sources and analysis

-  Proven ability to lead projects autonomously in a matrix environment

-  Track record of managing priorities and performance targets

Additional requirements may include:

-  Oncology Specific: Experience in oncology observational studies, experience in Flatiron and ConcertAI, understanding of programming logic in lines of therapy

-  Molecular Epi Specific:

- CCloud-based SQL is desirable

- Experience with Clinico-genomic multi-modal data (e.g. Tempus AI) or population biobank data (UK biobank)

- Experience and comfort to multitasking and working in a matrix environment

- Tableau or Power BI or other graphics tool is a plus

-  HEOR Specific:

- SAS/SQL required, additional experience with R beneficial

- Experience with health economics and outcomes research (HEOR) methodologies, including cost analysis, burden of illness studies, and comparative effectiveness research

At  Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range:

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.

**Get to know Syneos Health**

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

**Additional Information**

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Sr Biostatistician-Sr Data Scientist/Analyst (US and UK Only)

Industry: Software Development
Company Size: 51-200 employees

Netrolynx AI

**About The Company**

Harnham is a leading specialized recruitment and consulting firm dedicated to connecting top-tier talent with innovative organizations across data, analytics, and digital domains. With a strong global presence and a reputation for excellence, Harnham partners with clients in various industries including healthcare, life sciences, finance, and technology. The company's mission is to deliver tailored staffing solutions that drive business success and foster long-term partnerships. Harnham prides itself on its deep industry expertise, extensive network, and commitment to understanding each client’s unique needs, ensuring the placement of highly qualified professionals who can make a meaningful impact.

**About The Role**

The Clinical Data Scientist role at Harnham offers an exciting opportunity for professionals passionate about transforming clinical data into actionable insights. This hybrid or remote position is integral to supporting the final stages of clinical data pipelines within a growing organization focused on healthcare and life sciences technology. The successful candidate will be responsible for converting raw clinical datasets into standardized, analysis-ready formats suitable for clinical research and regulatory submissions. Collaborating closely with cross-functional teams—including Clinical Operations, Data Platform Engineering, and AI/ML teams—the Clinical Data Scientist ensures data accuracy, traceability, and regulatory compliance. This role provides a unique chance to work in a dynamic environment that emphasizes innovation, precision, and ethical data management, making a tangible impact on healthcare advancements.

**Qualifications**

Candidates should possess a BSc or MSc degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related field. A minimum of 2-5 years of experience in clinical data science, statistical programming, or clinical data management within pharmaceutical, biotech, or related environments is required. Technical proficiency in SAS, R, Python, and SQL is essential, along with familiarity with version control systems like Git. Experience working with CDISC SDTM/ADaM standards and understanding of oncology endpoints, such as RECIST and survival analysis, is highly desirable. Candidates with knowledge of real-world data (RWD) and NLP-derived outputs will have an added advantage. Strong analytical skills, meticulous attention to detail, and excellent communication abilities are critical for success in this role.

**Responsibilities**

Data Transformation & Delivery: Convert raw, manually abstracted, and AI-processed clinical data into standardized formats such as CDISC SDTM and ADaM, or client-specific data models. Build analysis-ready datasets from diverse sources including electronic medical records (EMRs), electronic data capture (EDC) systems, and internal abstraction tools, ensuring data integrity and consistency.

Statistical Programming & Reporting: Develop and generate comprehensive Tables, Listings, and Figures (TLFs) for clinical study reports and interim analyses utilizing SAS, R, or Python. Collaborate with statisticians and clinical teams to ensure accurate representation of data insights.

Data Integrity & Quality Control: Conduct thorough data cleaning, validation, and discrepancy investigations to differentiate between true clinical variability and upstream data errors. Maintain high standards of data quality and traceability throughout the process.

Cross-Team Collaboration: Partner with engineering teams to automate data cleaning, validation workflows, and improve data infrastructure. Serve as an internal customer and early tester for new data tools and systems, providing feedback to optimize performance and usability.

Documentation: Create and maintain detailed documentation including data specifications, derivation logic, reviewer guides, and Define.xml files. Ensure compliance with regulatory standards and facilitate audits and submissions.

Ad Hoc & Exploratory Analysis: Support internal and external stakeholders with data queries, exploratory analyses, and insights to demonstrate the value of the data platform. Contribute to data-driven decision-making processes across the organization.

Ethical & Compliant Data Management: Follow all applicable privacy, security, and compliance regulations such as HIPAA. Promote ethical handling of sensitive clinical data and uphold organizational standards for confidentiality and data protection.

**Benefits**

Harnham offers a competitive salary package commensurate with experience and qualifications. The role includes eligibility for equity, annual performance bonuses, and a comprehensive benefits package that encompasses health insurance, retirement plans, and professional development opportunities. The organization fosters a collaborative and inclusive work environment that values innovation and continuous learning. Flexible work arrangements, including hybrid or fully remote options, are available to support work-life balance. Employees gain exposure to cutting-edge healthcare data projects, enabling career growth and development within a supportive and forward-thinking organization.

Equal Opportunity

Harnham is committed to fostering an inclusive environment where diversity is valued and all individuals are treated with respect. We are proud to be an equal opportunity employer and do not discriminate based on race, ethnicity, gender, age, sexual orientation, disability, or any other legally protected status. Our hiring practices are designed to ensure fairness and equal access to employment opportunities for all qualified candidates. We believe that diverse teams drive innovation and excellence, and we are dedicated to creating a workplace where everyone can thrive and contribute to our shared success.

Data Scientist

**About The Company**

Harnham is a leading global recruitment firm specializing in data, analytics, and digital transformation talent acquisition. With a strong presence across multiple regions, Harnham is dedicated to connecting innovative organizations with top-tier professionals in the healthcare, life sciences, finance, marketing, and technology sectors. Our commitment to excellence and deep industry expertise enable us to deliver tailored staffing solutions that drive business success and foster long-term partnerships. Harnham prides itself on fostering a diverse, inclusive environment and maintaining high standards of integrity, professionalism, and customer satisfaction.

**About The Role**

We are seeking a highly skilled Clinical Data Scientist to join our client’s dynamic team, supporting the critical final stages of their clinical data pipeline. This hybrid or remote role offers an exciting opportunity to work within a forward-thinking organization committed to advancing healthcare through innovative data solutions. The ideal candidate will have a passion for transforming complex clinical datasets into analysis-ready formats that facilitate impactful research and regulatory submissions. You will collaborate closely with cross-functional teams, including Clinical Operations, Data Platform Engineering, and AI/ML specialists, to ensure the highest standards of data accuracy, traceability, and compliance are maintained throughout all deliverables.

**Qualifications**

Applicants should possess a Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related field. Candidates should have a minimum of 2-5 years of experience working in clinical data science, statistical programming, or clinical data management within pharmaceutical, biotech, or related environments. Technical proficiency in SAS, R, Python, and SQL is essential, along with familiarity with CDISC SDTM/ADaM standards. Experience with version control tools such as Git, understanding of oncology endpoints like RECIST and survival analysis, and exposure to real-world data (RWD) are highly desirable. Strong analytical skills, attention to detail, and excellent communication abilities are critical for success in this role.

**Responsibilities**

In this role, you will be responsible for transforming raw, manually abstracted, and AI-processed clinical data into standardized formats such as CDISC SDTM/ADaM or client-specific data models. You will build analysis-ready datasets from diverse sources, including electronic medical records (EMRs), electronic data capture (EDC) systems, and internal abstraction tools, ensuring data integrity and quality. Developing and generating Tables, Listings, and Figures (TLFs) for clinical study reports and interim analyses using SAS, R, or Python will be a core part of your work.

You will perform comprehensive data cleaning and validation checks, investigating discrepancies to differentiate between true clinical complexities and upstream data errors. Collaborating with engineering teams, you will help automate data workflows, enhancing efficiency and consistency. You will serve as an internal customer and early tester for new data infrastructure tools, providing feedback to improve system capabilities.

Documentation is vital; you will create and maintain detailed data specifications, derivation logic, reviewer guides, and Define.xml files to support audits and regulatory submissions. Supporting internal and external stakeholders through ad hoc data queries, exploratory analyses, and insights will demonstrate the value of the data platform. Ensuring compliance with privacy, security, and regulatory standards such as HIPAA is paramount, promoting ethical handling of sensitive clinical data.

**Benefits**

Our client offers a comprehensive benefits package designed to support your professional growth and personal well-being. This includes a competitive salary commensurate with experience and qualifications, opportunities for equity participation, annual performance bonuses, and a range of health and wellness benefits. Employees gain access to ongoing training and development programs, fostering continuous learning and career advancement. The organization also promotes a flexible work environment, with options for hybrid or fully remote work, enabling a healthy work-life balance. Additional perks include paid time off, retirement savings plans, and support for professional certifications.

Equal Opportunity

Harnham is an equal opportunity employer committed to fostering an inclusive environment for all employees and applicants. We do not discriminate based on race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, or any other protected characteristic. We believe in creating a diverse workforce that reflects the communities we serve and encourages innovation through varied perspectives. All employment decisions are made based on qualifications, merit, and business needs.

At Merck, known as MSD outside of the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.merck.com. 

This site is intended for residents of the United States and Canada and their territories only. FLS: http://merck.us/3TKXNuZ

Industry: Pharmaceutical Manufacturing
Company Size: 10,001+ employees

Merck

**Job Description**

In 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 (SDS QM), 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 SDTM

- Participation in industry teams and conferences on best practices

- Membership on departmental strategic initiative project teams

**Skills**

**Education and Minimum Requirement:**

- BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment

- MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial environment

**Department Required Skills And Experience**

- Effective interpersonal skills and ability to negotiate and collaborate effectively

- Effective written, oral, and presentation skills

- Effective 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 stakeholders

**Position Specific Required Skills And Experience**

- US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables.

- In-depth knowledge of and direct experience implementing industry clinical data standards (e.g., Controlled Terminologies, CDISC CDASH, SDTM, ADaM, and HL7) and submission deliverables (e.g., SDRG, ADRG, Define.xml).

- Proficiency in diverse data collection methods, including eCRF, IRT, and central lab data

- Demonstrated success in the assurance of deliverable quality and process compliance.

- Excels in technical writing, able to convert complex ideas and information into simple readable form

- Solid project management skills

- Strategic thinking - ability to turn strategy into tactical activities

- Ability to anticipate stakeholder requirements

**Preferred Skills And Experience**

- Strong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)

- Experience assuring consistency across protocols and projects

- Ability and interest to work across cultures and geographies

- Knowledge of clinical data metadata & information management platforms and systems.

- Experience using SAS, R, and Python to generate data-driven insights

- Ability to complete statistical programming deliverables through the use of global outsource partner programming staff

- Experience developing and managing a project plans in Microsoft Project or similar tools

- Active participation in professional societies

- Experience leading or contributing to process improvement initiatives

eligibleforERP

SPjobs

BARDS2020

VETJOBS

EBRG

**Required Skills**

Accountability, Clinical Trials, Data Management, Data Modeling, Electronic Submissions, Information Systems Management, Innovation, Machine Learning (ML), Microsoft Project, Numerical Analysis, Process Improvement Projects, Process Improvements, Project Management, Regulatory Compliance, REMOTE_SKILL-1-52891, Stakeholder Relationship Management, Statistical Programming, Technical Writing, Waterfall Model

**Preferred 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.

**Requirements**

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

**U.S. Hybrid Work Model**

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$117,000.00 - $184,200.00

This 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**

Regular

**Relocation:**

Domestic

**VISA Sponsorship**

Yes

**Travel Requirements**

10%

**Flexible Work Arrangements**

Hybrid

**Shift**

Not Indicated

**Valid Driving License**

No

**Hazardous Material(s)**

n/a

**Job Posting End Date**

04/12/2026

- 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: **R382409

Sr. Scientist, Statistical Programmer, Submission Data Standards Quality Management (Hybrid)

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