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Clinical Data Manager Jobs in Minnesota (NOW HIRING)

MN

$45 - $47/hr

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk ...

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk ...

The Associate Clinical Data Manager is responsible for performing data management tasks within defined established processes throughout the life cycle of the study including startup, conduct and ...

The Associate Clinical Data Manager is responsible for performing data management tasks within defined established processes throughout the life cycle of the study including startup, conduct and ...

The Manager, Clinical Data Review will exercise judgment in planning, organizing and performing work; monitor performance and report statuses to executive management as well as assures that quality ...

The Manager, Clinical Data Review will exercise judgment in planning,organizingand performing work;monitorperformance and report statuses to executive management as well as assures that quality of ...

The Manager, Clinical Data Review will exercise judgment in planning,organizingand performing work;monitorperformance and report statuses to executive management as well as assures that quality of ...

Join our team as a Clinical Assistant/DataEntry supporting a critical Epic EHR Data Abstraction ... Valuable experience with Epic and health information management * Collaborative and supportive work ...

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Clinical Data Manager information

See Minnesota salary details

$19

$55

$80

How much do clinical data manager jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for clinical data manager in Minnesota is $55.99, according to ZipRecruiter salary data. Most workers in this role earn between $44.28 and $66.63 per hour, depending on experience, location, and employer.

What are some common challenges clinical data managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

What are the key skills and qualifications needed to thrive as a clinical data manager?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What does a clinical data manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What does a clinical data manager do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

What are the most commonly searched types of Clinical Data jobs in Minnesota? The most popular types of Clinical Data jobs in Minnesota are:
What are popular job titles related to Clinical Data Manager jobs in Minnesota? For Clinical Data Manager jobs in Minnesota, the most frequently searched job titles are:
What cities in Minnesota are hiring for Clinical Data Manager jobs? Cities in Minnesota with the most Clinical Data Manager job openings:
Infographic showing various Clinical Data Manager job openings in Minnesota as of July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $116,461 per year, or $56 per hour.

$45 - $47/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago


Abbott rating

7.9

Company rating: 7.9 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

160th of 536 rated manufacturers


Job description

Apply Category: Healthcare & Clinical, Clinical Title: Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk-based quality management systems, as described in the risk assessment, data management plan, and site and central monitoring plans. As the customer-face of Data Review and its primary liaison with the therapy group, the Clinical Data Manager's therapy-specific knowledge ensures alignment to customer definitions of criticality, and informs review and analysis of study data. Main Responsibilities: Identification of study specific risks to study conduct and human subject safety; analysis of risks; development and implementation of mitigation strategies.

Review of study data to detect anticipated and unanticipated issues related to trial data completeness and quality. Facilitate multi-stakeholder discussions to review findings, evaluate impact and develop action plans for correction and continued monitoring. Conduct Central Monitoring activities, as described in Central Monitoring Plan.

Direct all data cleaning activity related to assigned studies. Education Level: Bachelors Degree ( 16 years) Biology, Health Sciences, Mathematics, Computer Science, or equivalent. Experience Details: 3 years in clinical operations or healthcare related field.

Education and work experience in project management, life sciences and/or technical field. Knowledge of data collection best practices for clinical trials. Knowledge of global clinical operations.

Experience in consultative role, with Subject Matter Expertise, and effectively influencing a team decision to the desired outcome. Proficient at the identification of risks in a process, evaluation of likelihood and impact, and the development of effective mitigation and monitoring strategies that are imperfect yet meet the business need. Proficient in the translation of clinical trial requirements to the technical specifications required for effective data collection.

Skilled at making inferences and connections based on limited information, clearly describing the knowns, unknowns, and alternative explanations. Intermediate project management skills; developing a multifaceted plan with complex dependencies and holding peers accountable to adherence to the plan while maintaining positive and collaborative relationships. Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device.

Consultants Eligible Benefits Upon Waiting Period: Medical and Prescription Drug Plans Dental Plan Vision Plan Health Savings Account (for High-Deductible Health Plans) Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit) Supplemental Life Insurance Short Term Disability (coverage varies by state) Long Term Disability Critical Illness, Hospital coverage, Accident Insurance MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance 401(k) Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives.

Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs. Published on 18 Jul 2026, 3:44 AM


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