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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in statistical programming and data analysis within clinical trials, with a strong focus on SAS and R programming. Capable of leading programming activities, ensuring high-quality deliverables, and collaborating effectively with cross-functional teams.
Highest-signal resume keywords
Statistical ProgrammingSAS ProgrammingR ProgrammingCDISC ComplianceData Integration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Statistical ProgrammingSASRSAS Macro LanguageData ValidationDerived DatasetsStatistical Analysis PlansElectronic SubmissionData Transfer SpecificationsSDTM/ADaM Specifications
Soft Skills
Strong Communication SkillsTechnical GuidanceCollaboration
Industry Keywords
Clinical TrialsPharmaceutical IndustryDrug Development ProcessCRO ManagementExploratory Analyses
About the role
Key responsibilities & impact- Lead statistical activities for clinical trials.
- Independently perform programming tasks and oversee programming deliverables.
- Provide technical guidance to other programmers.
- Program and validate derived datasets, tables, figures, and listings.
- Process data from external sources.
- Perform ad hoc exploratory analyses for publications and support other R&D functions.
- Oversee programming work and deliverables from CROs.
- Contribute to the design, implementation, and review of Case Report Forms, Data Transfer Specifications, Statistical Analysis Plans, SDTM/ADaM specifications, and Define packages.
- Program and validate CDISC-compliant electronic submission deliveries.
- Support creation of submission documentation.
- Ensure programming deliverables are timely and high quality.
- Help manage internal contractors and external vendors.
- Participate in developing departmental work instructions and guidelines.
- Help create enhanced functions, macros, and utilities.
- Collaborate with cross-functional teams and external vendors.
Requirements
What you’ll need- Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline.
- BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry.
- Working knowledge of SAS and its various components.
- Knowledge of R programming in clinical trials.
- Familiarity with the drug development process.
- Strong SAS and SAS Macro language skills.
- Strong knowledge of industry standards.
- Ability to work on data integrations (ISS and ISE).
- Strong oral and written communication skills.
- Ability to communicate analysis details to team members with less technical experience.
Benefits
Comp & perks- Professional growth opportunities
- Continuous training and development
- Equal opportunity and inclusive workplace
- Permanent role