Merck & Co, Inc

Senior Scientist, Stat. Programming, Late-Stage Development (Hybrid)

Merck & Co, Inc$117K — $184K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • BA/BS in relevant field or MS with applicable SAS experience in clinical trials
  • 5-7 years SAS programming experience for BA/BS holders, 3-5 years for MS holders
  • Significant expertise in SAS programming including advanced techniques
  • Demonstrated ability to manage projects and collaborate with stakeholders
  • Experience with CDISC and ADaM standards

Responsibilities

  • Develop and validate programming for analysis and reporting deliverables
  • Maintain project plans and manage resource forecasting
  • Coordinate activities of global programming teams including outsourced staff
  • Collaborate effectively with statistics and other project stakeholders
  • Lead statistical programming for the entire product lifecycle

Benefits

  • Hybrid work model allowing flexibility
  • Domestic relocation assistance offered
  • Visa sponsorship available for qualified candidates
  • Membership in professional societies encouraged
  • Opportunities for process improvement and collaboration across global teams
Full Job Description
Job Description

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 teams


Education Minimum Requirement:
  • 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 environment

OR
  • 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


Required Experience and Skills:

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:
  • 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


Preferred Experience and Skills:
  • Working knowledge or R programming languages for data analysis, automation, and clinical data standards activities
  • 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
  • Experience developing and managing a project plan using Microsoft Project or similar package
  • Active in professional societies
  • Experience in process improvement


BARDS2020

eligibleforERP

SPjobs

VETJOBS

EBRG

Required Skills:
Clinical Development, Clinical Trials, Data Management, Data Modeling, Numerical Analysis, Outcomes Research, Project Leadership, Project Management, SAS Macros, Software Development, Stakeholder Relationship Management, Statistical Programming

Preferred Skills:
R Programming, Team Commitment, Team Player, Willingness to Learn

Current Employees apply HERE

Current Contingent Workers apply HERE

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:
07/31/2026
*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.

About Merck & Co, Inc

Schering-Plough Corporation is a major U.S.-based manufacturer of pharmaceuticals. It operates in three segments: Prescription Pharmaceuticals, Animal Health, and Consumer Health Care. Schering-Plough develops products targeting on allergy, cancer, hepatitis, cardiovascular, central nervous system, respiratory system, and more.  It was founded in 1851 by Ernst Christian Friedrich Schering as Schering AG in Germany. Schering-Plough manufactured several pharmaceutical drugs, the most well-known of which were the allergy drugs Claritin and Clarinex, an anti-cholesterol drug Vytorin, and a brain tumor drug Temodar. It also developed drugs targeting on central nervous system and the respiratory system. Schering Plough also owned and operated the major foot care brand name Dr. Scholl's and the skin care line Coppertone. These also became a part of the new company. Schering-Plough was a full member of the European Federation of Pharmaceutical Industries and Associations (EFPIA), a membership which is also maintained by the new Merck.

Merck & Co, Inc Careers

Join the visionary team at Merck & Co, Inc, a global leader in healthcare dedicated to advancing the world of medicine. As part of our professional community, you'll find dynamic job opportunities that foster innovation and leadership across various fields. Merck & Co, Inc is not just a company; it's a place where you can make a difference.

Work You’ll Do

At Merck & Co, Inc, we are committed to improving global health through groundbreaking research and innovative healthcare solutions. Our team is at the forefront of developing new therapies and vaccines that significantly impact public health worldwide. By joining us, you will collaborate with some of the brightest minds in the industry, using your skills to contribute to projects that save and improve lives around the globe.

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Merck & Co, Inc is an ideal environment for those who lead with curiosity and the drive to innovate. Our leadership is committed to fostering a culture where inventive thinking and collaboration are encouraged, making it a perfect place for professionals who seek to make an impact through their work.

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We understand that our employees are our greatest asset, which is why we offer competitive benefits designed to support the health and well-being of you and your family. From comprehensive health care coverage and retirement plans to flexible working conditions and wellness programs, our benefits package is designed to meet the diverse needs of our team members.

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Learn more about Merck & Co, Inc
Size
68,000 employees
Market Cap
$282.6 billion
Industry
Net Income
$7 billion
Founded
1668
5 Year Trend
+4.1%
Revenue
$47.9 billion
NASDAQ

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