Senior Statistical Programmer - Clinical Trials
Merck & Co.
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Job summary
Merck & Co. in Rahway, NJ is seeking a Senior Scientist in Statistical Programming to support late-stage drug and vaccine clinical development.
You will develop and execute analysis and reporting deliverables, design statistical datasets, and collaborate with project teams to ensure timely, high-quality results across trials and regulatory submissions. The role requires a Master’s or Bachelor's degree with extensive SAS programming experience in a clinical trial setting, plus strong knowledge of
Qualifications
- Master's degree (or US equivalent) plus 3 years SAS programming in a clinical trial environment OR Bachelor's degree (or US equivalent) plus 5 years SAS programming in a clinical trial environment.
- Experience with CDISC and ADaM standards.
- Expertise in SAS programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database experience.
Responsibilities
- Provide support to statistical programming activities for late-stage drug/vaccine clinical development projects.
- Develop and execute statistical analysis and reporting deliverables from individual trials to global regulatory submissions.
- Design and maintain statistical datasets for multiple stakeholder groups across development, outcomes research and safety.
- Lead one or more projects and collaborate with statistics and other stakeholders to ensure timely, high-quality deliverables.
Skills
Education
Job description
Merck & Co. in Rahway, NJ is seeking a Senior Scientist in Statistical Programming to support late-stage drug and vaccine clinical development.
You will develop and execute analysis and reporting deliverables, design statistical datasets, and collaborate with project teams to ensure timely, high-quality results across trials and regulatory submissions. The role requires a Master’s or Bachelor's degree with extensive SAS programming experience in a clinical trial setting, plus strong knowledge of
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