Manager Clinical Databases & Integrations

Medtronic•Minneapolis, MN
•$136,000 - $204,000•Remote

About The Position

The Medtronic Clinical Research Solutions (MCRS) Clinical Compliance & Development organization provides database development, implementation, interface management, testing, and compliance support for clinical research across Medtronic. Its Development and Interface team works with Clinical Operations, Data Management, Data & Safety Management, and Operating Unit stakeholders to deliver clinical database solutions, maintain system integrations, and support clinical studies. The Manager, Clinical Databases & Integrations leads teams responsible for database development, implementation, and clinical systems integrations supporting Medtronic clinical research. The role provides operational leadership, resource management, process ownership, and strategic direction, ensuring high-quality, compliant, and scalable clinical data solutions. This position is remote in the United States, and the ideal candidate can support Eastern Time Zone business hours.

Requirements

  • Bachelor's degree and at least 5 years of experience in clinical data management, clinical database development, clinical systems implementation, or clinical research operations; alternatively, an advanced degree and at least 3 years of experience.
  • Experience managing clinical database platforms, clinical data systems, or clinical system integrations in a regulated environment.
  • For baccalaureate degrees earned outside the United States, a degree satisfying the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

Nice To Haves

  • Experience managing global teams across multiple geographic regions.
  • Experience leading people, supervisors, or cross-functional teams supporting clinical research processes.
  • Experience with clinical development processes, clinical data collection, testing, validation, and quality management requirements.
  • Experience developing and implementing process improvements, operational standards, or compliance-related initiatives.
  • Experience supporting electronic data capture (EDC) systems, clinical trial management systems (CTMS), or related clinical technology platforms.
  • Knowledge of Good Clinical Practice (GCP), regulatory compliance requirements, and clinical quality management systems.
  • Experience with resource planning, operational metrics, capacity management, and service delivery oversight.
  • Experience within medical device, pharmaceutical, contract research organization (CRO), or other regulated clinical research environments.

Responsibilities

  • Lead and develop database development, implementation, and interface management teams supporting clinical research operations.
  • Manage resource allocation, workload prioritization, and team capacity planning to meet quality, timeline, and budget objectives.
  • Serve as the business process owner for database development and clinical systems integration processes, driving standardization and continuous improvement.
  • Oversee clinical database development, implementation, testing, and system integration activities supporting clinical studies.
  • Maintain Development and Interface standard operating procedures, quality documentation, and process controls to ensure regulatory compliance.
  • Monitor operational metrics, forecasts, and delivery performance to identify risks and implement corrective actions.
  • Partner with Clinical Research, Data & Safety Management, Information Technology, and Operating Unit stakeholders to support delivery excellence and business continuity.
  • Lead resolution of complex operational issues, escalations, and cross-functional challenges affecting database development and interface services.

Benefits

  • Competitive salary and flexible benefits package.
  • Short-term incentive through the Medtronic Incentive Plan (MIP).
  • Health, dental, and vision insurance for eligible regular employees working 20 or more hours per week.
  • Health Savings Account and Healthcare Flexible Spending Account for eligible regular employees working 20 or more hours per week.
  • Life insurance and long-term disability leave for eligible regular employees working 20 or more hours per week.
  • Dependent daycare spending account and tuition assistance or reimbursement for eligible regular employees working 20 or more hours per week.
  • Simple Steps global well-being program for eligible regular employees working 20 or more hours per week.
  • Incentive plans for regular employees.
  • 401(k) plan with employer contribution and match for regular employees.
  • Short-term disability, paid time off, and paid holidays for regular employees.
  • Employee Stock Purchase Plan and Employee Assistance Program for regular employees.
  • Non-qualified Retirement Plan Supplement, subject to IRS earning minimums.
  • Capital Accumulation Plan, available to Vice Presidents and above or subject to IRS earning minimums.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service