Sr. Scientist, Stat. Programming - Late-Stage (Non-Oncology) (Hybrid)
$117k - $184.2kMSD Malaysia
- # Sr. Scientist, Stat. Programming - Late-Stage (Non-Oncology) (Hybrid)Applyremote type: Hybridlocations: USA - Pennsylvania - North Wales (Upper Gwynedd): USA - New Jersey - Rahwaytime type: Full timeposted on: Posted Todaytime left to apply: End Date: July 25, 2026 (14 days left to apply)job requisition id: R406345**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.This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more 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 datasets 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.**Primary Activities:*** Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices* Maintain and manage a project plan including resource forecasting* Coordinate the activities of a global programming team that includes outsource provider staff* Membership on departmental strategic initiative team**Educational Qualifications:*** BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 5 years SAS programming experience in a clinical trial environmentOR* MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 3 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 Skills and Experience:*** Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise* Designs and develops complex programming algorithms* Ability to comprehend analysis plans which may describe methodology to be programmed; an understanding of statistical terminology and concepts* Familiarity with clinical data management concepts* Experience in CDISC and ADaM standards* Experience ensuring process compliance and deliverable quality* 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* Ability to anticipate stakeholder requirements**Preferred Experience and Skills:*** Experience using R for statistical modeling, data analysis, and visualization* Demonstrated success in the assurance of deliverable quality and process compliance. Strong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)* US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables* Experience assuring programming consistency across protocols and projects, directing the program development effort of other programmers; experience as a programming mentor* Ability and interest to work across cultures and geographies* Ability to complete statistical programming deliverables through the use of global outsource partner programming staff* Developing and managing a project plan using Microsoft Project or similar package* Active in professional societies* Experience in process improvementBARDS2020eligibleforERPSPjobsVETJOBSEBRG**Required Skills:**CDISC ADaM, Clinical Data Interchange Standards Consortium (CDISC) Standards, Clinical Development, Clinical Trials, Computer Science, Data Management, Data Modeling, Life Science, Numerical Analysis, Process Improvements, Project Leadership, Project Management, SAS Graphs, Stakeholder Relationship Management, Statistical Analysis Systems (SAS) Programming, Statistical Programming, Waterfall Model**Preferred Skills:**Multiple Therapeutic Areas, Python (Programming Language), R ProgrammingCurrent Employees apply HERECurrent 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 RightsEEOC GINA SupplementWe 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 ActsThe 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 can apply for this role through (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:**07/25/2026**\*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.**Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
- J-18808-Ljbffr MSD Malaysia
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