Clinical SAS programmer job Waltham Massachusetts
Clinical SAS programmer job Waltham Massachusetts
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Clinical SAS programmer Job



Employer Name: SpiderID: 8718935
Location: Waltham, Massachusetts Date Posted: 6/7/2019
Wage: Category: Medical/Health
Job Code:

Job Description:
Responsibilities:

Responsible for overseeing the successful operation of one or more groups within Biostatistics.
Maintains responsibility for all assigned projects and direct reports. May also be expected to mentor associate managers, along with other employees.
It is also expected that the individual participates in informal business development activities.
Develops SAS programs to generate listings, tables and figures as outlined by mock TLF shells
Performs quality control (source code review, double-programming and log review) of SAS programs
Develops SAS programs to generate CDISC and other analysis data sets as outlined by respective specifications
Prepares specifications for CDISC and other analysis data sets
Assists Data Management with SAS programming needs
Acts as Lead Biostatistical Programmer to interact with the Lead Biostatistician and the study team


Job Requirements:
Requirements:
BS or equivalent from accredited college or university, in statistics, IT, mathematics or closely related field or work-related experience to be able to perform this role
8+ years of experience in SAS programming within the area of clinical trials
Prior experience using computerized information systems preferred
Knowledge of ICH and local regulatory authority drug research and development regulations preferred
Demonstrated working knowledge of data processing, database design and organization in clinical data environment
Demonstrated working knowledge of basic clinical trial design and analysis principles
Working knowledge of CDISC standards and application of these standards to projects
Working knowledge and understanding of advanced statistical concepts to program analysis datasets and tables which include descriptive and standard/complex inferential statistics.
Fluent verbal and written English as well as the local language(s) required for clinical trial submissions.
Excellent team player, collaborative and able to build an effective team
Ability to multitask and work effectively in a fast-paced environment with changing priorities.
Is customer service focused in approach to work both internally and externally
Maintains a positive, results orientated work environment.
Ability to build client confidence and achieving high levels of customer satisfaction
Attention to detail and ability to independently work on stand-alone Biostatistical projects with general supervision
Must have proven experience with Pharmacokinetic (PK) datasets and analyses
Practical experience as lead programmer for pharmacology studies preferred.


Contact Information:
Contact Name: Laxmi Sushobhita Company Type: Staffing Agency
Company: Intellectt
City: Reston
State: Virginia
Zip: 20170

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