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Senior/Principal Statistical Programmer Consultant

ClinChoice

Freelance / Contract
Canada
programmer
sas
statistics
math
data management
Apply for this position

 

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 searching for a Senior/Principal Statistical Programmer Consultant to join one of our clients. 

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.  

Main Job Tasks and Responsibilities: 

Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings;

Produce data listings, summary tables, and graphics for interim and final analyses;

Integrate data across studies within a project. Test, document, review, and validate all programs according to department guidelines;

Coordinate data transfer and/or programming standards with CROs and vendors. Validate analysis datasets and TFLs from vendors;

Collaborate with other Biometrics functions for all activities related to the analysis of clinical trial data;

Responsible for the execution of ad-hoc requests, manuscripts, posters, and presentations.

Requirements:

Minimum of 10 years of SAS programming in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, math, or MA/MS with 8 years of experience;

Expertise in SAS programming language, report generation, and standards for programming and validation;

Therapeutic area- Rare Disease

Experience with CDISC data standards required.

Experience as a senior statistical programmer at a pharmaceutical or CRO working in an FDA-regulated environment;

Experience with Clinical Study Reports and NDA submission;

Ability to work on multiple tasks simultaneously and meet project deadlines;

Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment.

 

 

ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity.  We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 (647)724-5709 x 301. 

We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ('PIPEDA') , personal information is collected under the authority of the Act and will only be used for candidate selection.

#LI-TT1 #LI-Remote #Principal#Contract

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About the job

Freelance / Contract
Canada
Posted 14 hours ago
programmer
sas
statistics
math
data management

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Senior/Principal Statistical Programmer Consultant

ClinChoice

 

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 searching for a Senior/Principal Statistical Programmer Consultant to join one of our clients. 

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.  

Main Job Tasks and Responsibilities: 

Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings;

Produce data listings, summary tables, and graphics for interim and final analyses;

Integrate data across studies within a project. Test, document, review, and validate all programs according to department guidelines;

Coordinate data transfer and/or programming standards with CROs and vendors. Validate analysis datasets and TFLs from vendors;

Collaborate with other Biometrics functions for all activities related to the analysis of clinical trial data;

Responsible for the execution of ad-hoc requests, manuscripts, posters, and presentations.

Requirements:

Minimum of 10 years of SAS programming in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, math, or MA/MS with 8 years of experience;

Expertise in SAS programming language, report generation, and standards for programming and validation;

Therapeutic area- Rare Disease

Experience with CDISC data standards required.

Experience as a senior statistical programmer at a pharmaceutical or CRO working in an FDA-regulated environment;

Experience with Clinical Study Reports and NDA submission;

Ability to work on multiple tasks simultaneously and meet project deadlines;

Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment.

 

 

ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity.  We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 (647)724-5709 x 301. 

We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ('PIPEDA') , personal information is collected under the authority of the Act and will only be used for candidate selection.

#LI-TT1 #LI-Remote #Principal#Contract

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