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

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)

Find Biostatistician jobs in New Jersey, United States with Savvy's AI Recruiter. Browse opportunities from top companies and get matched with roles that match your skills using our intelligent recruitment system.