ZipRecruiter

Log In

1

Clinical Data Associate Jobs in Savage, MN (NOW HIRING)

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

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 ...

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

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 ...

next page

Showing results 1-20

All JobsClinical Data Associate JobsClinical Data Associate Jobs in Savage, MN

Clinical Data Associate information

See Savage, MN salary details

$14

$41

$92

How much do clinical data associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical data associate in Savage, MN is $41.55, according to ZipRecruiter salary data. Most workers in this role earn between $31.30 and $41.54 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs

What cities near Savage, MN are hiring for Clinical Data Associate jobs?

Cities near Savage, MN with the most Clinical Data Associate job openings:

Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Savage, MN as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 2% Contract, and 1% Nights. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $86,424 per year, or $41.5 per hour.

Associate Clinical Data Manager

Abbott

Maple Grove, MN

Full-time

Medical, Retirement

Re-posted 14 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

169th of 545 rated manufacturers

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'llalso 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, theFreedom 2 Savestudent debtprogramandFreeUeducation benefit - an affordable and convenient path to getting a bachelor's degree.

  • A company recognized asa great placeto 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. Whetherit'sglucose 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 than10,000 peoplehave healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than500,000 peoplewith diabetes from routinengersticks.

The Opportunity-CAN CHANGE

Our locationinMapleGroveMNcurrently has an on-site opportunity for anAssociate Clinical Data Manager.TheAssociateClinical Data Managerisresponsibleforperformingdatamanagementtaskswithin defined established processes throughout the life cycle of the studyincluding startup,conductand reporting phases.

WhatYou'llWork On-CAN CHANGE

WorkswithData Review Managerin thestudystart-upandplanning, including contributing to the development oftheRiskAssessmentandRisk Mitigation Plan,Data Management Plan,Central MonitoringPlanand Data Review Plan.

TranslatesClinicalStudyrequirementsintotechnicalrequirementsforeCRFs,editchecks,studynotificationsandcustomizationsinthestudydatabasein close collaboration with othermemberof the data review team.

  • Able to developCRF with cross functional support, incorporatingappropriatefeedbackandfinalizingtheCRF.

  • Able to developspecifications fordatalistingsforcontinuous datareview,andcommunicate withdata analyticsteam membersthrough their development and release.

  • Able to work with external non-CRF data,including developingcreating Data Transfer Specifications,verification ofexternal data structure for import into thedata model.

  • Able to develop edit check specifications toreviewfor illogical,incompleteand inconsistent data includingtesting and troubleshooting ofeditschecks.

  • Identifies,analyzes,proposessolutions,andeffectivelyresolvescomplexdata/database structureissuesbyexercisingappropriatejudgmentandcollaboratingwiththeclinicalprojectteammembersandothersharedservicefunctions.

  • ContributestothedevelopmentandmaintenanceofClinicalDatabasesystems,includingEDC,EditChecks,Reporting,StudyNotifications,etc.throughthefollowing:

  • PartnercloselywithData ReviewManagement,StudyDatabaseManager, andDataAnalytics andSystemsand other Data Review team members.

  • Performanddocumentfunctionaland/oruseracceptancetestingonstudydatabases,reports,studynotifications,anddatabasecustomizations.

  • Utilizeexistingtools/reports,SQL,anddatabaseUItoidentifydataissuesanddriveresolutionswiththeClinicalStudyTeaminatimelymanner.

  • AttendClinicalStudyTeammeetings.

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

  • AssistsinFDAandQualitySystemauditsthatinvolveClinicalDatabaseandData Management

FollowsdatamanagementstandardsandbestpracticesandassuresStandardprocessesarefollowedforData Managementactivities.

Contribute todatacleaninganddatasnapshoteffortsforregulatorysubmissionsandotherbusinessneedsasrequestedbytheClinicalStudyTeamthroughthefollowing:

  • Generate databasesnapshotand prepare datasets forBiometrics.

  • Contribute todatareviewmeetingswiththeClinicalStudyTeamandBiometricstoidentifydatacleaningissuesandstrategizecleaningefforts.

  • Monitoroveralldatamanagementtaskstoensurethattimelinesaremetandthatanyissuesareproactivelyidentifiedandresolved.

Performotherdutiesasassigned.

Required Qualifications-CAN'TCHANGE

  • Bachelor's degree in a related fieldOR an equivalentcombinationof education and work experience.

  • Minimum3years'in clinical, medical or research setting.

  • Education and work experience in computer science, lifesciencesor technicalfield.

  • Knowledge of data collection best practices for clinical trials.

  • Knowledge of global clinical operations.

  • Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology,therapyand 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.

PreferredQualifications-CAN CHANGE

  • Bachelor'sdegree inbusiness administration, datascience,statisticsor life sciences.

  • 3years' experience inclinical operations or healthcare relatedfield.

  • KnowledgeofdatamanagementpracticesfromCRFdesigntodatabasedevelopmentandstudyclosure.

  • ExperiencewithusingElectronicData Capture(EDC)databasesandadvancedskill levelworking inExcel.

  • Knowledge of documentation practices in-line withGoodClinicalDataManagementPractices,andotherFDAregulationsandguidelinesisrequired.

  • Abilitytoleverageand/orengageotherstoaccomplishprojects.

  • Solidoralandwrittencommunicationskillsandanalytical/problem-solvingskills.

  • Mustbeabletoeffectivelymanagemultipleprojectsandtimelines.

  • Requirestheabilitytositorstandwhileworkingonacomputerforalongperiodoftime.

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 / StatisticsDIVISION:MD Medical DevicesLOCATION:United States > Maple Grove : 6820 Wedgwood Road N.ADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 5 % of the TimeMEDICAL SURVEILLANCE:NoSIGNIFICANT 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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

What Abbott employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply