Career Opportunities at iQuest

.Net Lead Engineer

.Net, MVC, C# with SQL knowledge developers with 5-8 years experience
Strong experience in developing applications with C#.Net, ASP.NET and ASP.Net MVC
Expertise in developing the services using WCF/Web API technologies
Good experience in writing T-SQL programming in SQL Server
Strong knowledge on Entity Framework, maintaining the multiple data sources
Strong knowledge on UI technologies using JQuery, Bootstrap, Ajax, AngularJS and CSS
Good in communication skills
Good in application integration skill with external systems
Excellent Communication and Analytical Skills
Good Team Player
Valid UK Visa (longterm) will be added advantage
Ready to travel onshore given the opportunity
Considering current situation Remote Working can be allowed

Minimum Experience of 2 to 4 yrs
Expertise in the SAS clinical programming and good understanding of the drug development process.
Perform Statistical Programming activities for the data summarization - program safety summary tables - listings for clinical studies. Have also been involved in the validation of the safety Tables and Listings.
Convert non-standard data to CDISC SDTM standard data model. Provide support for the submission activities.
Contribute to activities in validation and implementation including Standard Reporting Systems, SAS macro utility programs and associated tools. Contribute in development and implementation of programming standards and conventions.
Excellent Communication and Analytical Skills
Good Team Player
Valid UK Visa (longterm) will be added advantage
Ready to travel onshore given the opportunity
Considering current situation Remote Working can be allowed

Minimum Experience of 4 to 6 yrs
Good understanding of Clinical trial drug development processes and methodologies. Provide hands-on support to clinical projects across multiple therapeutic areas.
Provide strong technical programming support to the data standardization from non- standard data to CDISC SDTM standards.
Proven experience in development and update of in-house MACROs with strong programming efficiency and problem-solving skills.
Perform Statistical programming activities for data summarization/Statistical analysis which includes both safety and efficacy outputs and derived/analysis dataset.
Have also been involved in the validation of Analysis datasets, and the summary Tables and Listing.
Excellent Communication and Analytical Skills
Good Team Player
Valid UK Visa (longterm) will be added advantage
Ready to travel onshore given the opportunity
Considering current situation Remote Working can be allowed

Minimum Experience of 6+ yrs
Good understanding of the clinical drug development process.
Excellent knowledge of SAS programming and associated features and their applications in the pharmaceutical industry environment in particular clinical trial data setting.
Strong understanding of clinical trial data and extremely hands-on experience in analyzing them and being involved in reporting and submission of clinical trial data to the regulatory agencies.
Familiar with the SDTM and ADaM models and implement it in creating the specification based on the Statistical Analysis plan.
Generate the analysis dataset based on the specification and Perform Statistical Programming activities for the data summarization and validation of summary tables and listings for clinical studies.
Mentor Junior programmers and provide support on technical issues, processes and ensure compliance with the project level and company standards
Excellent Communication and Analytical Skills
Good Team Player
Valid UK Visa (longterm) will be added advantage
Ready to travel onshore given the opportunity
Considering current situation Remote Working can be allowed