Sr Clinical Business Intelligence Specialist

$106,400 - $159,600/Yr

Medtronic

Full-time - Mid Level

Remote

10,001+ employees

Miscellaneous Manufacturing

About the position

The position is part of Medtronic's Clinical and Regulatory Solutions (MCRS) team, specifically within the Data & Safety Solutions (DSS) and Solutions Design & Optimization (SDO) group. The role focuses on applying design and development expertise to create reports and custom components that support clinical trials. It involves collaboration with various internal and external stakeholders to ensure effective data management and reporting standards are met.

Responsibilities

• Plan, analyze, design, develop, test, deploy and/or support Clinical Reports, Clinical Data Transfer/Interfaces or other components related to the clinical studies.
• Understand and utilize industry standards to contribute to defining and implementing reporting standards for the development team.
• Support other Clinical Business Intelligence Specialists on planning, designing, and implementing Clinical Reports and Dashboards, Clinical Data Transfers/ Interfaces, or other components.
• Mentor junior team members.
• Understand the design of business unit and enterprise system datasets/databases and contribute to testing and/or supporting them.
• Partner as clinical technical specialists in the planning, designing, and implementing of clinical applications.
• May provide technical consultation on and task direction for vendors.
• Stay current on technologies, methods, standards, and best practices as well as trends and direction of the clinical data management industry.
• Review and acknowledge all Standard Operating Procedures and other quality requirements assigned to the job role.

Requirements

• Bachelor's degree plus 4+ years of development experience (2+ year with an advanced degree).

Nice-to-haves

• Bachelor's degree in Computer Science, IT, or Science.
• Clinical database knowledge: advanced level of proficiency with relational databases and clinical operations data.
• Knowledge of systems development life cycle and relational databases.
• Knowledge of documentation and validation practices as applicable to the development of software components in a clinical research or similarly regulated environment.
• Experience in developing reporting solutions in support to business processes in a clinical research or similarly regulated environment.
• Knowledge of ICH/GCP/FDA regulations and guidelines as they pertain to clinical systems including 21 CRF Part 11.
• Familiarity with SQL code development (intermediate to advanced database and query development).
• Familiarity with the Microsoft SQL Server suite, primarily MS SQL Reporting Services (intermediate to advanced solutions and report development).
• Familiarity with Microsoft Power BI (basic to intermediate dashboard development).
• Familiarity with SQL Server, Oracle Clinical, Siebel CTMS, Clinical Development Analytics and/or other SQL-based Databases and Clinical applications.
• Familiarity with project management practices (as needed to be able to co-lead and co-administer a project).

Benefits

• Competitive Salary
• Flexible Benefits Package
• Short-term incentive called the Medtronic Incentive Plan (MIP)