SAS Programmer jobs in Bangalore - vista global

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  • Job View 5 Views
  • Applicants Less than 5 Applicants
  • 2019-04-17

Job Description

The Study Data Tabulation Model (SDTM) Subject M

• Serve as an SDTM SME

• Collaborate with key stakeholders to understand dataset requirements for SDTM

• Accountable for the review of DB specifications related to SDTM.

• Accountable for execution of processes related to clinical trials SDTM, SDTM+ development, including specification, programming, QC, and deliverables of SDTM data for analysis and submission

• Engages appropriate stakeholders in communication to create SDTM standards and process for transition of clinical data to SDTM. Includes Data Transfer Specification review for external data

• Accountable for SDTM datasets specification, conversion, and delivery to stakeholders, specifically Statistical Programming, but also other users of SDTM datasets, with high quality and on time deliverables

• Provides SDTM data production technology consultation to client Clinical Data Operations related to SDTM data delivery and manages the activities of a team with a common focus

Basic Qualifications:

• Bachelor’s degree

• Minimum 5 years of relevant programming and drug development experience in Clinical Research Organization (CRO), Pharmaceutical or Biotech organizations (preferably in Phase I-IV trials)

• SDTM Subject Matter Expert

• Expertise in CDISC/SDTM standards and applicability to clinical database design/capture and reporting

• Excellent Statistical Analysis Systems (SAS) programming skills (at least 5 years SAS experience preferred)

• Expert knowledge in clinical trials with 5+ years’ experience working in a clinical project team environment

• Proven experience in development and implementation of clinical standards in a global pharmaceutical environment.

• Experience in consulting projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle preferred

• Knowledge of Pinnacle 21

• Experience in creating reviewer’s guides and Define.xml for SDTM

• Experience across Therapeutic Area

Key Skills

  • SAS Programming

Industry

Pharma/BioTech/Clinical Research

Functional Area

Pharma / R&D / Biotech

Number of Vacancy

10

Education

B.Pharma, B.Tech/B.E, M.Pharma


About vista global

The Study Data Tabulation Model (SDTM) Subject M
• Serve as an SDTM SME
• Collaborate with key stakeholders to understand dataset requirements for SDTM
• Accountable for the review of DB specifications related to SDTM.
• Accountable for execution of processes related to clinical trials SDTM, SDTM+ development, including specification, programming, QC, and deliverables of SDTM data for analysis and submission
• Engages appropriate stakeholders in communication to create SDTM standards and process for transition of clinical data to SDTM. Includes Data Transfer Specification review for external data
• Accountable for SDTM datasets specification, conversion, and delivery to stakeholders, specifically Statistical Programming, but also other users of SDTM datasets, with high quality and on time deliverables
• Provides SDTM data production technology consultation to client Clinical Data Operations related to SDTM data delivery and manages the activities of a team with a common focus
Basic Qualifications:
• Bachelor’s degree
• Minimum 5 years of relevant programming and drug development experience in Clinical Research Organization (CRO), Pharmaceutical or Biotech organizations (preferably in Phase I-IV trials)
• SDTM Subject Matter Expert
• Expertise in CDISC/SDTM standards and applicability to clinical database design/capture and reporting
• Excellent Statistical Analysis Systems (SAS) programming skills (at least 5 years SAS experience preferred)
• Expert knowledge in clinical trials with 5+ years’ experience working in a clinical project team environment
• Proven experience in development and implementation of clinical standards in a global pharmaceutical environment.
• Experience in consulting projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle preferred
• Knowledge of Pinnacle 21
• Experience in creating reviewer’s guides and Define.xml for SDTM
• Experience across Therapeutic Area

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