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Entry Level Clinical Data Analyst Jobs in Minnesota

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

Partner closely with Data Review Management, Study Database Manager, and Data Analytics and Systems ... Attend Clinical Study Team meetings. * Contribute technical expertise to cross functional teams ...

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

Partner closely with Data Review Management, Study Database Manager, and Data Analytics and Systems ... Attend Clinical Study Team meetings. * Contribute technical expertise to cross functional teams ...

Allina Health

Data Analyst

Minneapolis, MN · On-site +1

$32.92 - $45.12/hr

August 21, 2026 Department: 74000670 Clinical Engineering Services Management Shift: Day (United ... Hybrid remote position Supports a variety of data analysis, project management, and quality ...

AG Technologies

Data Analyst

Minneapolis, MN

... clinical data from Act as the primary resource to educate providers on the required file standards and submission processes Define record layouts and mapping documents to transform provider files to ...

Horizon Technologies Inc.,

Data Analyst

Minneapolis, MN · On-site

... clinical data from. Act as the primary resource to educate providers on the required file standards and submission processes. Define record layouts and mapping documents to transform provider files ...

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How much do entry level clinical data analyst jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for entry level clinical data analyst in Minnesota is $35.61, according to ZipRecruiter salary data. Most workers in this role earn between $28.70 and $41.20 per hour, depending on experience, location, and employer.

What is an entry level clinical data analyst?

An Entry Level Clinical Data Analyst is responsible for collecting, cleaning, and analyzing clinical data to support healthcare research and decision-making. They work with databases, statistical tools, and reporting software to ensure data accuracy and integrity. Their role often includes identifying trends, generating reports, and assisting in regulatory compliance. This position requires analytical skills, attention to detail, and knowledge of clinical terminology and data management systems. It is a great starting point for individuals interested in healthcare analytics and clinical research.

What are the typical daily responsibilities of an entry level clinical data analyst?

As an Entry Level Clinical Data Analyst, your daily responsibilities typically include reviewing and cleaning clinical trial data, performing data entry or validation tasks, generating standard reports, and assisting with database testing and documentation. You may work closely with senior data analysts, clinical research coordinators, and project managers to ensure data accuracy and compliance with regulatory standards. Collaboration and communication are key, as you’ll often participate in team meetings to discuss data queries or project updates. This hands-on experience helps build a strong foundation for future growth in the clinical data management field.

What are the key skills and qualifications needed to thrive as an entry level clinical data analyst?

Entry Level Clinical Data Analysts need foundational knowledge in statistics, data management, and healthcare terminology, usually supported by a degree in a related field such as life sciences, health informatics, or mathematics. Familiarity with data analysis software like Microsoft Excel, SAS, or SQL, and exposure to clinical trial management systems or electronic data capture (EDC) platforms are beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this role. These competencies are crucial for ensuring accurate and reliable data collection, analysis, and reporting that directly support clinical research outcomes.

Can I become an entry level clinical data analyst with no experience?

Entry level clinical data analysts typically need a bachelor's degree in a related field such as health informatics, biology, or statistics. While prior experience is not always required, familiarity with data management tools like Excel or SQL and understanding of clinical research processes can improve job prospects. Entry-level roles often provide on-the-job training for specific software and procedures.

What do you need to be an entry level clinical data analyst?

To become an entry-level clinical data analyst, candidates typically need a bachelor's degree in health informatics, biology, statistics, or a related field. Skills in data management, proficiency with tools like Excel and SQL, and understanding of clinical trial processes are important. Some positions may also require familiarity with electronic data capture systems and basic knowledge of regulatory standards such as HIPAA.

What are the most commonly searched types of Clinical Data Analyst jobs in Minnesota?

The most popular types of Clinical Data Analyst jobs in Minnesota are:

What are popular job titles related to Entry Level Clinical Data Analyst jobs in Minnesota?

For Entry Level Clinical Data Analyst jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Entry Level Clinical Data Analyst jobs in Minnesota look for?

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Entry Level Clinical Data Analyst jobs near you
Infographic showing various Entry Level Clinical Data Analyst job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, 3% Contract, and 1% Nights. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $74,068 per year, or $35.6 per hour.

Associate Clinical Data Manager

Maple Grove, MN • On-site

Abbott

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

170th of 545 rated manufacturers

People enjoy working here

Good employer

Recommended by parents

Learn more about Abbottexternal

Full-time

Medical, Retirement

Re-posted 9 days ago

Job description

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, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
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.

For years, Abbott's medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it's glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies 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 finger sticks.
The Opportunity - CAN CHANGE
Our location in Maple Grove MN currently has an on-site opportunity for an Associate Clinical Data Manager. 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 reporting phases.
What You'll Work On - CAN CHANGE
Works with Data Review Manager in the study start-up and planning, including contributing to the development of the Risk Assessment and Risk Mitigation Plan, Data Management Plan, Central Monitoring Plan and Data Review Plan.
Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study notifications and customizations in the study database in close collaboration with other member of the data review team.
  • Able to develop CRF with cross functional support, incorporating appropriate feedback and finalizing the CRF.

  • Able to develop specifications for data listings for continuous data review, and communicate with data analytics team members through their development and release.

  • Able to work with external non-CRF data, including developing creating Data Transfer Specifications, verification of external data structure for import into the data model.

  • Able to develop edit check specifications to review for illogical, incomplete and inconsistent data including testing and troubleshooting of edits checks.

  • Identifies, analyzes, proposes solutions, and effectively resolves complex data/database structure issues by exercising appropriate judgment and collaborating with the clinical project team members and other shared service functions.

  • Contributes to the development and maintenance of Clinical Database systems, including EDC, Edit Checks, Reporting, Study Notifications, etc. through the following:

  • Partner closely with Data Review Management, Study Database Manager, and Data Analytics and Systems and other Data Review team members.

  • Perform and document functional and/or user acceptance testing on study databases, reports, study notifications, and database customizations.

  • Utilize existing tools/reports,SQL, and database UI to identify data issues and drive resolutions with the Clinical Study Team in a timely manner.

  • Attend Clinical Study Team meetings.

  • Contribute technical expertise to cross functional teams through CRF changes and the impact on databases and propose implementation strategies.

  • Assists in FDA and Quality System audits that involve Clinical Database and Data Management

Follows data management standards and best practices and assures Standard processes are followed for Data Management activities.
Contribute to data cleaning and data snapshot efforts for regulatory submissions and other business needs as requested by the Clinical Study Team through the following:
  • Generate database snapshot and prepare datasets for Biometrics.

  • Contribute to data review meetings with the Clinical Study Team and Biometrics to identify data cleaning issues and strategize cleaning efforts.

  • Monitor overall data management tasks to ensure that timelines are met and that any issues are proactively identified and resolved.

Perform other duties as assigned.
Required Qualifications - CAN'T CHANGE
  • Bachelor's degree in a related field OR an equivalent combination of education and work experience.

  • Minimum 3 years' in clinical, medical or research setting.

  • Education and work experience in computer science, life sciences or technical field.

  • Knowledge of data collection best practices for clinical trials.

  • Knowledge of global clinical operations.

  • Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device.

  • Intermediate medical knowledge related to common medical histories, medical terminology, diagnostics (imaging, laboratory), and medications (class, dose, route).

  • Certified Clinical Data Manager (CCDM) or equivalent.

Preferred Qualifications - CAN CHANGE
  • Bachelor's degree in business administration, data science, statistics or life sciences.

  • 3 years' experience in clinical operations or healthcare related field.

  • Knowledge of data management practices from CRF design to database development and study closure.

  • Experience with using Electronic Data Capture (EDC) databases and advanced skill level working in Excel.

  • Knowledge of documentation practices in-line with Good Clinical Data Management Practices, and other FDA regulations and guidelines is required.

  • Ability to leverage and/or engage others to accomplish projects.

  • Solid oral and written communication skills and analytical/problem-solving skills.

  • Must be able to effectively manage multiple projects and timelines.

  • Requires the ability to sit or stand while working on a computer for a long period of time.

The base pay for this position is
$61,300.00 - $122,700.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
MD Medical Devices
LOCATION:
United States > Maple Grove : 6820 Wedgwood Road N.
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 5 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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