MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS/R programming experience in a clinical trial environment Department Required ...
New
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS/R programming experience in a clinical trial environment Department Required ...
New
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS/R programming experience in a clinical trial environment Department Required ...
New
Rahway, NJ ยท Hybrid
Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS ... R, Python and XML experience * Experience with Linked data, natural language processing
Rahway, NJ ยท Hybrid
Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS ... R, Python and XML experience * Experience with Linked data, natural language processing
Expertise in clinical trial programming, including data manipulation, reporting workflows ... Clinical SAS Programming, Data Management, Data Modeling, Numerical Analysis, R Programming ...
Expertise in clinical trial programming, including data manipulation, reporting workflows ... Clinical SAS Programming, Data Management, Data Modeling, Numerical Analysis, R Programming ...
R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical ... As a biostatistical/SAS programmer I, you are responsible for the following tasks: * Develop SAS ...
Quick apply
R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical ... As a biostatistical/SAS programmer I, you are responsible for the following tasks: * Develop SAS ...
Somerset, NJ ยท On-site
$72K/yr
R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical ... As a biostatistical/SAS programmer I, you are responsible for the following tasks: * Develop SAS ...
Quick apply
Somerset, NJ ยท On-site
$72K/yr
R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical ... As a biostatistical/SAS programmer I, you are responsible for the following tasks: * Develop SAS ...
Basking Ridge, NJ ยท Remote
$95K - $204K/yr
... and R and/or SAS programming. * Excellent oral and written communication skills in English are a must. * Prior work experience in epidemiology, health economic and outcome research, or clinical ...
Quick apply
Basking Ridge, NJ ยท Remote
$95K - $204K/yr
... and R and/or SAS programming. * Excellent oral and written communication skills in English are a must. * Prior work experience in epidemiology, health economic and outcome research, or clinical ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Familiarity with clinical data management concepts * Strategic thinking - ability to turn strategy ...
The Senior Statistical Programmer, Submission Data Standards Quality Management (SDSQM), provides ... Familiarity with clinical data management concepts * Strategic thinking - ability to turn strategy ...
$119K - $222K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
$119K - $222K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
$119K - $222K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
$119K - $222K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
East Hanover, NJ ยท On-site
$119K - $222K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
East Hanover, NJ ยท On-site
$119K - $222K/yr
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming. Video Link ...
East Hanover, NJ ยท On-site +1
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming Video Link ...
East Hanover, NJ ยท On-site +1
SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming Video Link ...
In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP) * Expert in SAS or R programming, including the development and validation of ...
In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP) * Expert in SAS or R programming, including the development and validation of ...
In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP) * Expert in SAS or R programming, including the development and validation of ...
In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP) * Expert in SAS or R programming, including the development and validation of ...
In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP) * Expert in SAS or R programming, including the development and validation of ...
In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP) * Expert in SAS or R programming, including the development and validation of ...
In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP) * Expert in SAS or R programming, including the development and validation of ...
In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP) * Expert in SAS or R programming, including the development and validation of ...
Role Overview The Sr. Manager, Biostatistician/Programmer plays a critical hands-on role in ... Advanced proficiency in SAS for clinical trial analysis and reporting. * Working knowledge of R for ...
Role Overview The Sr. Manager, Biostatistician/Programmer plays a critical hands-on role in ... Advanced proficiency in SAS for clinical trial analysis and reporting. * Working knowledge of R for ...
Tarrytown, NY ยท On-site
As a Senior Clinical Pharmacologist this individual is expected to plan, design, implement and ... PD, E-R analyses (or work closely with Research Specialist or PMx Stats Programming team) to ...
Tarrytown, NY ยท On-site
As a Senior Clinical Pharmacologist this individual is expected to plan, design, implement and ... PD, E-R analyses (or work closely with Research Specialist or PMx Stats Programming team) to ...
Raritan, NJ ยท On-site
$76K - $121K/yr
Designing and developing programs in support of clinical analysis and reporting activities ... SAS, R, Python etc. is required. * Knowledge of processes, methods, and concepts relevant to ...
Raritan, NJ ยท On-site
$76K - $121K/yr
Designing and developing programs in support of clinical analysis and reporting activities ... SAS, R, Python etc. is required. * Knowledge of processes, methods, and concepts relevant to ...
Tarrytown, NY ยท On-site +1
As a Senior Clinical Pharmacologist this individual is expected to plan, design, implement and ... PD, E-R analyses (or work closely with Research Specialist or PMx Stats Programming team) to ...
Tarrytown, NY ยท On-site +1
As a Senior Clinical Pharmacologist this individual is expected to plan, design, implement and ... PD, E-R analyses (or work closely with Research Specialist or PMx Stats Programming team) to ...
Raritan, NJ ยท On-site
$76K - $121K/yr
Designing and developing programs in support of clinical analysis and reporting activities ... SAS, R, Python etc. is required. * Knowledge of processes, methods, and concepts relevant to ...
Raritan, NJ ยท On-site
$76K - $121K/yr
Designing and developing programs in support of clinical analysis and reporting activities ... SAS, R, Python etc. is required. * Knowledge of processes, methods, and concepts relevant to ...
| Aspect | Clinical R Programmer | Clinical SAS Programmer |
|---|---|---|
| Required Credentials | Typically requires a degree in statistics, biostatistics, or related field; proficiency in R programming | Usually requires a degree in statistics, biostatistics, or related field; proficiency in SAS programming |
| Work Environment | Often works in research-focused settings, academia, or biotech companies using open-source tools | Commonly employed in pharmaceutical companies, CROs, and clinical trial data analysis using SAS |
| Industry Usage | Growing in popularity for data analysis and visualization in clinical research | Standard in clinical trial data management and regulatory submissions |
While both roles involve programming for clinical data analysis, Clinical R Programmers focus on using R for statistical analysis and visualization, whereas Clinical SAS Programmers primarily use SAS for data management and reporting. The choice depends on the company's preferred tools and project requirements.
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted yesterday
Job Description
In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's 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.
Summary
Responsibilities:
This position provides high quality statistical programming deliverables for global stakeholders in Early Development Statistics and PK/PD Modeling and Simulation spanning all our Company's therapeutic areas except oncology. The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve required data, transform data into analysis/modeling datasets, and develop tables, listings and figures according to statistical/modeling analysis plan. The senior programmer will be a key collaborator with statisticians, modelers, and colleagues in other related function areas.
Primary Activities:
Prepare compliant programming code for regulatory submissions including analysis/modeling datasets, tables, listings, figures and associated documentation
Ensure programmatic traceability from data source to analysis/modeling result
Support the development of programming standards to enable efficient and high-quality production of programming deliverables
Skills
Education and Minimum Requirement:
BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS/R programming experience in a clinical trial environment OR
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS/R programming experience in a clinical trial environment
Department Required Skills and Experience:
Excellent communication (oral, written) skills, interpersonal skills and ability to negotiate and collaborate effectively
Effective knowledge and experience in developing analysis and reporting deliverables for research and development projects (data, analyses, tables, graphics, listings)
A project leader; completes tasks independently at project level
Position Specific Required Skills and Experience:
Programming expertise with clinical endpoint data (efficacy and safety)
Experience in CDISC SDTM and ADaM standards
If owns SAS programming experience, significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH
Designs and develops complex programming algorithms
Ability to comprehend analysis plans which may describe methodology to be programmed; understanding of statistical terminology and concepts; Implements statistical methods not currently available through commercial software packages.
Preferred Skills and Experience:
Programming expertise with pharmacokinetic data (raw concentration data, derived PK parameters)
Familiarity with clinical pharmacology concepts and pharmacokinetics concepts
Experience with at least one other software than SAS/R (e.g., Python, NONMEM)
Good working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)
Utilizes and contributes to the development of standard departmental SAS macros
Ability and interest to work across cultures and geographies
Ability to complete statistical programming deliverables through the use of global outsource partner programming staff
Active in professional societies
eligibleforERP
SPjobs
BARDS2020
VETJOBS
EBRG
Required Skills:
Accountability, Applied Engineering, Clinical Trials, Computer Science, Data Analysis, Data Management, Data Modeling, Mechatronics, Numerical Analysis, R Programming, Software Development, Stakeholder Relationship Management, Statistical Analysis Systems (SAS) Programming, Statistical Programming, Waterfall ModelPreferred Skills:
NONMEM, Pharmacokinetic Modeling, PKPD Modeling, Python (Programming Language), Translational Pharmacokinetics and Pharmacodynamics (PKPD)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
$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:
YesTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
06/24/2026*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.