Associate Principal Scientist, Statistical Programming

CareerCircle
Rahway, NJ, United States
16 days ago
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Role details

Contract type
Franchise
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
1 year minimum
Compensation
$145,475.0 - $224,100.0
Working hours
Regular working hours

Tech stack

Data Analysis Big Data Clinical Data Management Data Cleansing R (Programming Language) Commercial Software SAS (Software) Macros Information Technology Raster Graphics

Job description

Innovation Statistics Compassion SAS Macros Life Sciences SAS (Software) Clinical Trials Computer Science Pharmacokinetics Data Preprocessing Statistical Methods Applied Mathematics Statistical Modeling Statistical Programming R (Programming Language) User Requirements Documents Very Large Databases (VLDB) Arc Digitized Raster Graphic, * Provide high quality statistical programming analysis and reporting deliverables for global stakeholders, within our Research and Development division.

  • Gather and interpret user requirements for analysis and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into analysis/modeling datasets, and develop tables and figures according to statistical/modeling analysis plan.
  • Partner with stakeholders to solve problems and reduce the amount of programming tasks being completed by stakeholders to facilitate an increase in efficiency and compliance for statistical/modeling analyses.
  • Write programs to analyze data with statistical methods which are not currently available through commercial software packages. Act as key collaborator with statisticians, modelers, and colleagues in other related function areas., Innovation Statistics Compassion SAS Macros Life Sciences SAS (Software) Clinical Trials Computer Science Pharmacokinetics Data Preprocessing Statistical Methods Applied Mathematics Statistical Modeling Statistical Programming R (Programming Language) User Requirements Documents Very Large Databases (VLDB) Arc Digitized Raster Graphic +0 Associate Principal Scientist, Statistical Programming Merck & Co., Inc

Rahway, NJ*On-Site

Oncology Innovation Statistics Compassion SAS Macros Life Sciences SAS (Software) Clinical Trials Computer Science Pharmacokinetics Data Preprocessing Statistical Methods Applied Mathematics Statistical Modeling Statistical Programming R (Programming Language) User Requirements Documents Very Large Databases (VLDB) Arc Digitized Raster Graphic +0 Senior Scientist, Statistical Programming Merck & Co., Inc

Rahway, NJ*On-Site

Marketing Innovation Algorithms Statistics Compassion SAS Macros Life Sciences SAS (Software) Clinical Trials Computer Science Telephone Skills Outcomes Research Strategic Thinking Applied Mathematics Project Stakeholders Statistical Analysis Contingent Workforce Statistical Programming Pre-Clinical Development Clinical Data Management Interpersonal Communications +0 Login | JoinContact

Requirements

  • Master’s degree or equivalent in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 7 years of SAS/R programming experience in a clinical trial environment.
  • OR a Bachelor’s degree or equivalent in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years of SAS/R programming experience in a clinical trial environment.

Position Specific Required Skills and Experience:

Requires 7 years of experience with all of the following:

  • Experience in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, and SAS/GRAPH;
  • Experience in CDISC SDTM and ADaM standards;
  • Experience in preparing eSubmission packages including ADRG, XPT files, and Pinnacle 21 validation; and completing statistical programming deliverables through the use of global programming staff.

Requires 5 years of experience with all of the following:

  • Manipulating very large databases including complex data preprocessing, filtering, and manipulation;
  • Oncology franchise studies; applying oncology concepts; experience programming with oncology therapeutic area clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data and derived PK parameters);
  • Experence leading study programming deliverables for multiple studies.

Requires 1 year of experience with at least one software other than SAS (e.g., R).

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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