Job Overview
The Trial Informatics Senior Analyst supports the administration of the Veeva Clinical system and tools utilized by Development Operations. The Informatics Senior Analyst ensures standardization in the process for collection of metrics and data.
Essential Functions
1. Support the administration of reporting systems and prepare metric reports.
2. Work with clinical study teams to ensure the accuracy of data in clinical systems.
3. Provide support, under the direction of the TMF Compliance Manager, to Veeva Clinical end users, including receipt, evaluation and recommendation for all issue/enhancement requests. Hands-on training support as required.
4. Provide appropriate access to user requests to Veeva Clinical system.
5. Monitor and Support Integration functionality and administration with the partner Contract Research Organizations (CRO’s) to ensure data flow, record mapping, and record matching is occurring as expected.
6. Collaborate with the technical team as needed to support system enhancement and roll out of changes/enhancements.
7. Support the development of training material/user manuals/learning solutions for clinical systems.
8. Provide SharePoint Site Administration support to Clinical Study Support Team Sites and pages as needed or assigned by Department SharePoint Owner(s).
9. Support study teams and Dev Ops Leadership in making data-driven decisions to optimize clinical trial recruitment and Increase efficiency of study start up activities.
Qualifications
10. Bachelor Degree in an IT or scientific field.
11. Minimum 5 years of experience in the pharmaceutical industry related to support of clinical systems.
12. Previous Veeva Platform Knowledge preferred
13. General knowledge of and experience working in a GCP environment.
14. Demonstrate communication and technical writing skills.
15. Strong computer and analytical thinking skills.
16. Goal oriented, self-starter with proven ability to work independently.
17. Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines.
Skills Required
18. General knowledge of and experience working in a GCP environment
19. Demonstrated communication, influencing, collaboration and technical writing skills
20. Strong interpersonal skills and knowledge depth of subject matter to converse with vendors and internal functions
21. Demonstrated problem solving and strategic thinking skills
22. Goal oriented, self-starter with proven ability to work independently
23. Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines
24. Comfort with ambiguity; ability to act without having the total picture
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.