About this opportunity
abbott lists this Senior Manager, Study Data Architecture (on-site) opportunity in maple grove, Minnesota. Review the employer’s description below for duties, qualifications and application requirements.
Job description
JOB DESCRIPTION:
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.
We are recruiting a Senior Manager, Study Data Architecture to work on‑site at our Maple Grove, MN location. This role provides strategic and operational leadership to ensure high-quality, compliant, and efficient database configuration activities that support clinical trial execution and data collection objectives. The Senior Manager is accountable for the overall quality, consistency, and timely delivery of study database configuration activities across the clinical development portfolio, ensuring alignment with organizational objectives, data standards, and study execution timelines. The Senior Manager drives the implementation and governance of database standards, conventions, and processes across studies and programs while ensuring alignment with organizational data strategies. This position partners cross-functionally with Clinical Data Management, Clinical Data Analytics, Data Systems, and Study Management to ensure timely database delivery, consistency in data collection, and seamless support for downstream analytics and reporting.
What You’ll Work On
Leadership and People Management
Lead, mentor, and develop a team which fosters a culture of accountability, collaboration, continuous improvement, and operational excellence.
Establish team goals, performance expectations, and development plans aligned with departmental and organizational objectives.
Provide oversight of resource allocation, workload management, and capacity planning to support study and portfolio priorities.
Study Database Management Oversight
Accountable for the overall performance, quality, and timely delivery of study database configuration activities across the clinical development portfolio, proactively identifying risks, resolving resource constraints, and escalating issues as appropriate.
Oversee the planning, execution, and delivery of clinical study database builds across multiple studies and therapeutic areas.
Provide strategic guidance and issue resolution for complex database design and implementation challenges.
Standards, Governance, and Data Strategy
Establish and enforce database development standards, conventions, and best practices across all clinical programs, ensuring compatibility with analytical tools, reporting platforms, and internal applications.
Ensure clinical databases are aligned and mapped to organizational common data models to support downstream analytics, reporting, and regulatory submission requirements.
Lead continuous improvement initiatives focused on standardization, operational efficiency, quality, scalability, and automation.
Cross-Functional Collaboration
Ensure direct reports effectively collaborate with cross-functional study teams and internal stakeholders to support study execution and data collection objectives.
Oversee participation in protocol review, study planning, and study startup activities to ensure data collection requirements are accurately translated into database design and configuration.
Strategic Initiatives
Contribute to departmental strategy and long‑range planning related to database standards, technologies, operating models, and organizational capabilities.
Define and execute the strategic roadmap for study database management capabilities, including standards governance, technology adoption, process optimization, and organizational scalability to support the evolving needs of the clinical development portfolio.
Champion the adoption of organizational common data models and standardized data collection frameworks to improve consistency, reusability, and analytical readiness across the clinical development portfolio.
Required Qualifications
Associate’s degree
7 years’ related experience
Preferred Qualifications
Bachelor’s degree in life sciences, computer science information systems or related field or an advanced degree
8+ years’ years’ experience in data, systems or operations within healthcare, life sciences, clinical research, regulated industries and related environments
3+ years’ people leadership experience with demonstrated success developing, coaching and retaining high performing teams.
Experience leading teams responsible for data collection systems, database configuration, data operations, business systems, or comparable operational functions.
Demonstrated experience managing complex work portfolios, priorities, resources, and competing stakeholder needs
Experience implementing standards, processes, quality controls, and operational best practices.
Strong understanding of data quality, data governance, and data lifecycle concepts.
Experience working with common data models, data standards, or enterprise reporting and analytics teams.
Proven ability to lead teams through organizational, process, or technology change while maintaining employee engagement and performance.
Strong collaboration, communication, and stakeholder management skills.
Abbott is an Equal Opportunity Employer, committed to employee diversity.
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The base pay for this position is
$113,300.00 – $226,700.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Product Development
DIVISION:
MD Medical Devices
LOCATION:
United States > Maple Grove : 6820 Wedgwood Road N.
WORK SHIFT:
Standard
TRAVEL:
Yes, 10 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Awkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law link - English: is the Law link - Espanol:
#J-18808-Ljbffr
Worksite address
maple grove, MN, 55311, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.