At a Glance
- Tasks: Design and build clinical databases, ensuring top-notch quality and collaboration with diverse teams.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic work environment with potential for career advancement.
- Why this job: Make a real impact in healthcare by designing innovative solutions.
- Qualifications: Bachelor's degree and 2-4 years of relevant experience required.
The predicted salary is between 70000 - 115605 $ per year.
Responsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders - DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addition to project deliveries, the role also would be responsible for the project financials from programming shared services perspective.
Essential Functions
- Interprets the study protocol.
- Design and update the eCRF within Medidata RAVE and other platforms as required.
- Create and update Edit Specification Document.
- Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page).
- 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 lead discussions regarding the Edit Specification Document.
- Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.
- Escalate potential quality issues.
- Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures.
- Review build timelines and provide input as applicable.
- Review budgets for own projects, identify out of scope activities if any and inform relevant parties.
- Responsible for multiple study design projects at the same time.
- 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.
All responsibilities are essential job functions unless noted as nonessential (N).
Qualifications
- Bachelor’s Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology.
- 2-4 years of relevant RAVE designer experience and total experience being 7+ years.
Sr. Clinical DB Designer in Kirkland employer: IQVIA
IQVIA is an exceptional employer that fosters a dynamic work culture where innovation and collaboration thrive. Located in a vibrant area, employees benefit from access to cutting-edge resources and professional development opportunities, ensuring continuous growth in the consulting and analytics field. With a strong emphasis on mentorship and teamwork, IQVIA empowers its consultants to make meaningful contributions while enjoying a supportive environment that values their expertise and insights.
