Senior Statistical Programmer

About this role

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.

Responsibilities

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.

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