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GlaxoSmithKline Pharmaceuticals
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Senior Programming Lead
6-8 years
Bangalore / Bengaluru
1 vacancy
Senior Programming Lead
GlaxoSmithKline Pharmaceuticals
posted 9hr ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
- Involves in the development, validation, and review of study & standard programs/macros (Including SAS, CQL, PL/SQL, SPOTFIRE, R-Programming, Python) that support standard and study-level conversion of clinical trial data.
- Responsible for the review, development, and validation of SDTM mapping, aCRF, SDRG (Study Data Reviewers Guide), Pinnacle 21, define.xml, data Listings and checks for various standard or specific studies.
- Leads the Requirement gathering, development of specifications, validation plans and performing end to end validation of Standard/Study macros.
- Implements defensive programming techniques as a part of development lifecycle management of macros/programs/tools.
- Project Manages end to end study and ensures deliverables are met on time.
- Handles end to end studies (CDM (Clinical Data Management) To Submission).
- Support the programmers in troubleshooting and debugging of complex standard and study programs/macros.
- Acts as a technical owner and/or reviewer/approver for tools and programs developed in the group.
- For complex programs & tools, oversee & coordinate a group of Programming in a matrix setting.
- Establish and maintain effective working relationships with partners and stakeholders while assisting them through progress and challenges with deliverables.
- Adhere to the relevant departmental SOPs (Standard Operating Procedures), corporate policies, regulatory requirements, and industry best practices.
- Adhere to standards and aware of industry standards and updates.
Employment Type: Full Time, Permanent
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