26/03 Ashish
HR Executive at KonnectHR

Views:217 Applications:3 Rec. Actions:Recruiter Actions:0

Principal Statistical Programmer (4-17 yrs)

Bangalore/Hyderabad/Mumbai Job Code: 5974

We have career opportunity with Clinical Research Team at Mumbai,Bangalore & Hyderabad for below positions.

4 - 10 Years (Senior Statistical Programmer)

10 - 12 Years (Principal Statistical Programmer)

13- 17 yrs ( Manager

About Company:

Our client is global provider of biopharmaceutical services. It conducts clinical trials on behalf of its pharmaceutical clients to expedite the drug approval process. It is the largest clinical research organization in the world and has helped develop approximately 95% of the 200 top-selling biopharmaceuticals on the market today.

Qualification :

Minimum Requirements

- BA/BS/MS equivalent experience in mathematics, statistics, computer science, or health sciences/related field. Fluent English (oral and written).

- Advanced SAS experience and proven skills in the use of SAS within a Statistical Programming environment to develop and validate deliverables

- Advanced experience in contributing to statistical analysis plans and/or constructing technical programming specifications.

- TLF ( Tables, Listings & Figures) SAS coding Macros SQLPROC reports & with ADaM (Analysis Data Model) safety reports efficacy

(OR)

2nd Option is TLF (Tables, Listings & Figures) SAS coding with Efficacy and Safety report studies and any related Analysis Data Model experience.

- Good understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, study procedures).

- Good communications and negotiation skills, ability to work well with others globally

- Experience as Trial Programmer, including coordination of internal or external programmers on a given study/project

- Ideally 4+years of work experience in a programming role preferably supporting clinical trials/ or in pharmaceutical industry.

Job Responsibility:

1) Lead statistical programming activities as a statistical Programmer for either a large/pivotal study or several studies, or act as a Lead/Program Programmer

2)Co-ordinate activities of all programmers either internally or externally assigned to the study/project work, mentor other programmers in functional expertise and processes. Make statistical programming decisions/recommendations at study or project level.

3)Build and maintain effective working relationship with cross-functional teams, able to summarize and discuss status of deliverables and critical programming aspects (timelines, scope, resource plan), e.g. as member of the extended Clinical Trial Team (CTT).

4)Provide and implement statistical programming solutions; ensure knowledge sharing.

Expertise :

TLF ( Tables, Listings & Figures) SAS coding Macros SQLPROC reports & with ADaM (Analysis Data Model) safety reports efficacy

(OR)

2nd Option is TLF (Tables, Listings & Figures) SAS coding with Efficacy and Safety report studies and any related Analysis Data Model experience.

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