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urgent need STATISTICAL RPOGRAMMER at Remote, Remote, USA
Email: [email protected]
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=2063366&uid=

From:

abhisek.k,

source Infotech Inc

[email protected]

Reply to: [email protected]

STATISTICAL RPOGRAMMER

LONG TERM CONTRACT

100% REMOTE OPPORTUNITY

The Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal partnering functions, collaborators, and external functional service providers to ensure all the programming results are delivered in timely manner with high quality.

In this role, a typical day might include the following:

Lead programming support within multiple studies/projects in various study activities to ensures timely and high-quality programming deliverables in assigned projects and areas. Develop and maintain programming documentations and specifications following programming standards and processes

Demonstrate company values by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability

Understand the scope of work, plan and complete the deliveries and timelines with the study team, programming lead and management

Support global regulatory authority submissions including preparing programming deliverable for submission and working closely with partnering functions to address health authority requests.

This role may be for you if have:

Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills.
Knowledge of other programming languages such as R, Python etc. is a plus.

Good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles). Knowledge of regulatory submissions and requirements is a plus

SAS, (Base, Stat, Macro, graph)

; SAS certificates a plus

To be considered for this opportunity you must have:

MS. (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 5+ years of programming experience preferably in processing
clinical trial data in the biotechnology, pharmaceutical or health related industry.

Abhishek kumar

IT Recruiter

Desk No

:

6062299047 , Ext- 124

Email:

[email protected]

Hangout:
abhishekchoudhary0948

Source InfoTech Inc.

3840 Park Avenue, Suite C-205, Edison, NJ-08820

Keywords: cprogramm active directory rlang information technology microsoft New Jersey
urgent need STATISTICAL RPOGRAMMER
[email protected]
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=2063366&uid=
[email protected]
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12:15 AM 09-Jan-25


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