Senior Statistical Programmer

ClinChoice ANZ; United States; On-site; USD 90,000 - 140,000; Full time

Job summary

ClinChoice is hiring a Senior Statistical Programmer to lead statistical strategy for clinical trials in a permanent role. You will program and validate datasets, tables, figures, and listings, and oversee CRO deliverables.

You will contribute to SDTM/ADaM specifications, Define packages, and CDISC submissions, while supporting documentation and vendor management. Strong SAS and R skills are essential for success in this role.

Qualifications

• 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 of the drug development process.
• Strong SAS and SAS Macro language skills.
• R programming skils in clinical trials
• Strong knowledge of industry standards.
• Ability to work on data integrations (ISS and ISE).
• Strong oral and written communication skills. Ability to communicate details of the analysis to other team members with less technical experience.

Responsibilities

• Program and validate derived datasets, tables, figures, listings. Process data from the external sources.
• Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations.
• Oversee programming work/deliverables from CROs.
• Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.
• Program and validate CDISC compliant deliveries for the electronic submissions.
• Support in the creation of supporting documentation for submissions.
• Ensure programming deliverables are on time and of high quality.
• Help managing internal contractors and external vendors.
• Participate in development of departmental working instructions and guidelines.
• Help in creation of enhanced functions/macros and utilities.

Education

Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline

Tools

SAS

R

SAS Macro language

Job description

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds...

ClinChoice is currently recruiting for a Senior Statistical Programmer to join our team in a permanent position - an exciting opportunity to lead impactful statistical strategy in a dynamic environment.

Programing for clinical trials

• Program and validate derived datasets, tables, figures, listings. Process data from the external sources.
• Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations.
• Oversee programing work/deliverables from CROs.
• Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.

Electronic Submissions

• Program and validate CDISC compliant deliveries for the electronic submissions.
• Support in the creation of supporting documentation for submissions.

Project Management

• Ensure programming deliverables are on time and of high quality.
• Help managing internal contractors and external vendors.

Standards And Guidelines

• Participate in development of departmental working instructions and guidelines.
• Help in creation of enhanced functions/macros and utilities.

Qualification & Experience

• 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 of the drug development process.
• Strong SAS and SAS Macro language skills.
• R programming skils in clinical trials
• Strong knowledge of industry standards.
• Ability to work on data integrations (ISS and ISE).
• Strong oral and written communication skills. Ability to communicate details of the analysis to other team members with less technical experience.

Who will you be working for?

About ClinChoice

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.