Prog-Tester Lab Data Mgmt 2 (R1079642) in Bangalore, India at IQVIA™

Date Posted: 7/10/2019

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Job Description

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation, Q2 Solutions uses its global experience and scientific expertise to transform science and data into actionable medical insights that help customers improve human health.  A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organization’s clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it.

Provide comprehensive technical expertise in team environment responsible for development and maintenance of Laboratory Data Management (LDM) systems or the development of extraction tools from laboratory data management systems to meet internal and external client’s needs.  

• Serve as Lead Programmer or tester for database design, testing, implementation, or business reporting.
• Plan and coordinate database design, development, and testing for regional or transnational use.  
• Provide technical expertise to the Laboratory Data Management programming and testing team.  
• Ensure that databases and database extraction processes are documented in accordance with SOPs and reported in a timely fashion to support operations.
• Provide technical expertise to internal and external clients.
• Program, test, and document databases in accordance with programming standards and validation procedures.
• Mentor other team members in training and developing technical and/or database expertise.
• Independently bring solutions to the Laboratory Data Management teams.
• May assist IT in evaluating and/or developing and implementing new technologies
• May assist in developing, revising, and maintaining core operating procedures and working instructions with LDM management.
• Meet assigned milestones and interact with the project team to organize timelines, responsibilities and deliverables.
• Develop and maintain good communications and working relationships with teams and external clients.
• May interact with the Central Laboratories team to negotiate timelines, responsibilities, and deliverables.

• Programming Specific:
• Plan and coordinate database design, development, and implementation of laboratory data systems
• Program database manipulations and data extracts for internal and external clients.
• Supports the creation of libraries of reusable project specific programming that can be reused.

• Testing Specific:
• Plan and coordinate the testing plan and test cases of laboratory data systems, data extractions or business reports
• Assist in the creation of test data to support test case execution and supports creation and maintenance of libraries of reusable test data sets.
• Review specifications and requirements for testability and very traceability of testing to requirements.
• Understand and comply with core standard operating procedures and working instructions.
• Utilize multiple communication styles and skills to effectively broker audience specific [peers, senior team members, internal/external customers] business and interpersonal relationships that leads to positive outcomes and successful business results.

• Advanced knowledge of multiple programming languages such as C, C#, SSL, VGL, SQL, and SAS
• Solid understanding of laboratory data management systems and the clinical drug development process.
• Strong customer-focus perspective with skill to guide customer communications and customer management.
• Self-driven; keen attention to detail to anticipate, address and/or escalate issues, with aptitude to embrace and be conduit for change.
• Project and task management capabilities to meet/exceed deliverables.
• Effective problem solving skills as well as ability to proactively identifying process improvements which reduce operational costs and maintain quality.
• Quality conscious with high degree of ethics and integrity carrying out duties in accordance to laws, regulatory standards, and with company policies and procedures. 
• Proven leadership skills
• Demonstrated ability to manage multiple projects and tasks simultaneously.
• Computer proficiency including word processing, spreadsheet and Power Point applications.
• Good understanding of medical, clinical research, and Lab Data Management process and terminology.
• Knowledge on elicitation of the data requirements and authoring specifications.
• Knowledge on various regulatory requirements such as FDA, ICH, ISO HL7, and GLP (Good Laboratory Practices).

Job ID: R1079642


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