Clinical Statistical SAS programmer New Jersey

monfrair Clinical SAS Programmer 0 Comments

Clinical Statistical SAS programmer New Jersey
Full-time position located in North, NJ
No Sponsorship or relocation available
Apply for the position at the end of this post.

Clinical Statistical SAS programmer New Jersey

Job Description Senior Statistical Programmer Excellent opportunity for a pharmaceutical company that’s a strong and growing newcomer in the US. They are very well-funded and established overseas and are making a big commitment to become a fully integrated company here. The company has a strong pipeline, three drugs in Phase 3 and three drugs entering Phase 2, among others. Since they are in Start-up mode in the US, it’s a somewhat relaxed, informal atmosphere – and it’s an opportunity to join them at an exciting time and to make a big contribution and grow with the company. The company has an extraordinarily team-focused culture and provides 100% company-paid health benefits and company-provided lunch for all employees on a daily basis. Responsibilities: The Senior Statistical Programmer is responsible for the statistical programming efforts for specific projects and studies, including developing, testing, maintaining, validating, and documenting SAS programs. As part of the Statistical Programming team, provide technical expertise to the development of SAS programming standards and procedures.
• Generate, validate, and/or review TFL to support the statistical analysis of clinical trial data in support of regulatory submissions and publications.
• Generate, validate, and/or review SDTM domains and datasets and associated specifications and documents.
• Generate or perform quality control for SAS programs and other study documents (e.g., presentations and reports).
• Maintain complete and auditable documentation of all programming activities.
• Review datasets and output across SAS programs and studies to ensure consistency.
• Provide statistical programming support to supplemental or exploratory analyses for regulatory agencies, or any other internal and external ad-hoc requests.
• Assist in programming, testing, and documenting SAS global utility programs and tools in accordance with standards and validation procedures.
• Participate in the development and/or maintenance of departmental procedures and standards
• Review CRFs, edit check specifications, and TFL shells; assist in of TFL shell under of statisticians.
• Participate in monitoring CRO activities and reviewing CRO deliverables as necessary. Requirements:
• Bachelor’s degree in Statistics, Mathematics, or Computer Science or related field.
• Minimum of 5 years Pharma/CRO experience as a clinical trial SAS Programmer.
• Knowledge of Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS
• Knowledge of industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines.
• Excellent organizational skills, time management, and ability to meet deadlines.
• Excellent communication and interpersonal skills to effectively interface with others.
• Ability to work effectively across a matrix organization.
• Ability to work independently and collaboratively. Company Description They are very well-funded and established overseas and are making a big commitment to become a fully integrated company here. The company has a strong pipeline, three drugs in Phase 3 and three drugs entering Phase 2, among others. Since they are in Start-up mode in the US, it’s somewhat relaxed, informal atmosphere and it’s an opportunity to join them at an exciting time and to make a big contribution and grow with the company. The company has an extraordinarily team-focused culture and provides 100% company-paid health benefits and company-provided lunch for all employees on a daily basis.

Clinical Statistical SAS programmer New Jersey

Check out all of our openings at www.exigrp.com
contact the recruiter directly at bill@exigrp.com

You can apply in the comments section below.

 

Clinical Statistical SAS programmer New Jersey

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