Sr. Scientist, Statistical Programming (Hybrid)

Merck Sharp & Dohme LLC
North Wales, United States of America
2 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English
Experience level
Senior
Compensation
$ 184K

Job location

North Wales, United States of America

Tech stack

Data analysis
Computer Programming
R
Python
Commercial Software
SAS (Software)
Software Engineering
Information Technology
Modeling and Simulation
Data Management

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 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

Requirements

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, 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 Model

Preferred Skills:

NONMEM, Pharmacokinetic Modeling, PKPD Modeling, Python (Programming Language), Translational Pharmacokinetics and Pharmacodynamics (PKPD)

Benefits & conditions

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 (https://www.msdprivacy.com/us/en/CCPA-notice/)

The salary range for this role is

$117,000.00 - $184,200.00

About the company

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.

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