wwwLathaHR.com Clinical SAS Developer for a long term Remote Contract role, Pharma Client- Phone Hire

 Hi,

       Hope you are doing good, I have a REMOTE job for SAS programmer role. Please send me your available candidates.

 

Job Description: _REMOTE CLINICAL SAS DEVELOPER

Phone Hire

Completely Remore job

Long term contract

Sr. SAS Clinical Programmer

op 3-5 Skills: 1. SAS Programming 2. Good communication 3. Previous exp. working in pharm/biotech biometrics and stat programming environment 4. Ability to work independantly with limited supervision 5. BS or equivalent work experience

 Food and Drug Administration (FDA) Compliance-Experienced-2, Regulatory Policy and Controls Compliance-Experienced-2, Statistics: Knowledge-Expert-2


Description:
Provides clinical programming technical leadership and expertise to client project teams.
Reviews and implements project specifications to ensure meeting project deliverables and timelines.
Reviews and implements project validation activities to ensure quality of final deliverables
Supports development of study metadata utilized in submission of electronic data packages.
Works directly with client staff on Biometrics and CDISC data conversion submissions projects.
Designs, develops, evaluates and modifies SAS programs to analyze and evaluate clinical data (Statistical Programming Focus)
Designs, develops and validates CDISC data conversion specifications, data definition files and annotated case report forms (CDISC Analyst Focus)
Technically support the preparation of Biometrics deliverables including, but not limited to, submission CRT databases, tables, listings
and graphs for clinical study reports, statistical data packages (Statistical Programming Focus)
Ensures timely completion of regulatory submissions.
Assists in the development and maintenance of departmental SOPs, policies, and work instructions.
Compliance with all department metrics reporting and tracking systems
Support, as needed, department management in the preparation of Proposals and Statements of Work contracts.
Client site visits and travel to other CSC site may be required.

Qualifications
• Excellent written and oral communication skills (English).
• Extensive SAS experience in a Clinical environment. Minimum 7 years. (Statistical Programming Focus)
• Operational CDISC conversion experience. Minimum 5-7 years (CDISC Analyst Focus)
• Expertise in CDISC data standards including the SDTM, ADaM and SEND models. (CDISC Analyst Focus)
• Able to demonstrate a strong understanding of CDISC standards. (Both focuses)
• Hands-on experience with SDTM programming within FDA submission.
• Hands-on experience with ADaM programming within FDA submission.
• Hands-on experience with reporting programming within FDA submission
• Able to demonstrate excellent knowledge of particular SAS programming skills such as
 Macros
 SQL
 SAS Graph
 Proc Report
 SAS Stat
• Strong working knowledge of electronic data submission requirements including data definition preparation and aCRF development. (Statistical Programming Focus)
• Advanced working knowledge of electronic data submission requirements including data definition preparation and aCRF development. (CDISC Analyst Focus)
• Experience in writing and adhering to SOPs.

• Interview job applicants
• Recommending candidates for hire
• Counseling and coaching junior staff
• Support the evaluation of work processes
• Answering questions related to work methods
• Work experience with a US company.
• Educated in US.
• SAS certification (Statistical Programming Focus)
• CDISC training (CDISC Analyst Focus)

 

Thanks & Regards,

Lav Yadav
Source Infotech Inc.
3840 Park Avenue, Suite C-20, Edison, NJ, 08820
EMAIL: lyadav@sourceinfotech.com
Phone: 646.216.8084 | Fax: 732-909-2282 | Gtalk: lav.okaya

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