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Senior Technical Design Analyst – Bloemfontein

  • Bloemfontein
  • Anywhere

Senior Technical Design Analyst

IQVIA

Bloemfontein, BEN

http://jobs.zeleus.com/D158ED15EE4F45EF9960EF6AD4815C7723

**RESPONSIBILITIES**

+ Oversees timely and quality delivery of study deliverables.

+ Interprets the study protocol.

+ Design and update the eCRF.

+ Create and update Edit Specification Document.

+ Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page)

+ Complete the Study Authorization Form and Trial Capacity Request Form (InForm)

+ Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting. Attend and present comments at the Internal Design Review Meeting. May lead Online Screen Review Meeting.

+ Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document.

+ Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates.

+ Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.

+ Identify, escalate and propose solutions for potential quality issues.

+ Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures for self and other TDs within the team.

+ Reviews build timelines and provide input as applicable.

+ Reviews QIP for own projects, identify out of scope activities if any and inform relevant parties.

+ Oversee budget and financial performance of multiple TD studies within scope and inform relevant parties as required.

+ Design Library Source Study and Create Edit Specifications for source study.

+ Support other TDs in studies based on their therapeutic area expertise.

+ Mentors and trains new TDs in the team.

+ May contribute/assist Manager in resource planning for TD projects.

+ Act as SEM for TD role.

+ Responsible for multiple study design projects at the same time.

+ Might be working on projects across multiple platforms.

+ Identify areas for process improvements on an ongoing basis. Actively take part and contribute towards process improvement initiatives as assigned besides providing suggestions for continuous improvement of processes.

**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**

Bachelor in Science/Computer science/Information Technology or Bachelor in Technology with about 7 to 9 years of core CDM experience OR equivalent combination of education and experience.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

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