RadCube Careers
Systems Administrator/Senior
A single full time and dedicated resource will work as part of Lilly led team to deploy the initial production instance of the ClinRun SaaS solution. The Supplier resource shall be able to meet the following minimum criteria:
• Self managing in day to day tasks, needing minimal tactical and technical guidance once acclimated to the IGP initiative.
• 10 years experience designing and developing cross-organizational data interfaces both from the data content and transport technology perspectives.
• Demonstrated ability to call out and negotiate technical specifications with various tech-savvy counterparts – i.e. listen and influence others to achieve alignment.
• Skilled at summarizing and explaining technical topics (e.g. designs, constraints, trade offs) with non-technical stakeholders.
• Means of solicitating and/or raising key technical requirement gaps for team consideration.
• Experience testing complex system integrations within a quality management system including drafting quality documentations and authoring/executing test cases in support of system validation.
• General professional preparedness – i.e. prompt to meetings, timely communications, meet agreed upon deadlines.
• Working knowledge of clinical operational data concepts.
The Suppler resource will additionally:
• use a Lilly supplied computer for engagement work,
• be assigned relevant training and complete all training on time,
• work a standard day based upon US East Coast Timezone expectations and be available 5 days/week unless previous arrangement are made with Lilly team staff, and
• be available for in-person meetings held at Lilly Corporate Center as needed (note: it is expected that in-person meetings will be rare if the Resource resides outside the Indianapolis area).
1. Project Deliverables
• Lilly-ClinRun interface data element specifications and associated data transformation logic.
• Data transfer specifications (DTS) between Lilly and the ClinRun environments.
• Design, development and testing of the Lilly-side transport mechanisms; note that development in the ClinRun environment is out of scope and up to 3 APIs/file drop interfaces are currently foreseen.
• Documentation of interface designs.
• Test environment definition and participation in its provisioning.
• Quality documentation as required to fulfill CSQA validation activities including:
o Jira stories/requirements
o Design documentation.
o Test plans, test scripts, test execution, test summary reports.
o Security, maintenance and recovery plans.
• Participation in meetings and working sessions as required.
• Self managing in day to day tasks, needing minimal tactical and technical guidance once acclimated to the IGP initiative.
• 10 years experience designing and developing cross-organizational data interfaces both from the data content and transport technology perspectives.
• Demonstrated ability to call out and negotiate technical specifications with various tech-savvy counterparts – i.e. listen and influence others to achieve alignment.
• Skilled at summarizing and explaining technical topics (e.g. designs, constraints, trade offs) with non-technical stakeholders.
• Means of solicitating and/or raising key technical requirement gaps for team consideration.
• Experience testing complex system integrations within a quality management system including drafting quality documentations and authoring/executing test cases in support of system validation.
• General professional preparedness – i.e. prompt to meetings, timely communications, meet agreed upon deadlines.
• Working knowledge of clinical operational data concepts.
The Suppler resource will additionally:
• use a Lilly supplied computer for engagement work,
• be assigned relevant training and complete all training on time,
• work a standard day based upon US East Coast Timezone expectations and be available 5 days/week unless previous arrangement are made with Lilly team staff, and
• be available for in-person meetings held at Lilly Corporate Center as needed (note: it is expected that in-person meetings will be rare if the Resource resides outside the Indianapolis area).
1. Project Deliverables
• Lilly-ClinRun interface data element specifications and associated data transformation logic.
• Data transfer specifications (DTS) between Lilly and the ClinRun environments.
• Design, development and testing of the Lilly-side transport mechanisms; note that development in the ClinRun environment is out of scope and up to 3 APIs/file drop interfaces are currently foreseen.
• Documentation of interface designs.
• Test environment definition and participation in its provisioning.
• Quality documentation as required to fulfill CSQA validation activities including:
o Jira stories/requirements
o Design documentation.
o Test plans, test scripts, test execution, test summary reports.
o Security, maintenance and recovery plans.
• Participation in meetings and working sessions as required.
