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Clinical Data Associate Jobs in New Hope, 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 ...

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 ...

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Clinical Data Associate information

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How much do clinical data associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical data associate in New Hope, MN is $40.47, according to ZipRecruiter salary data. Most workers in this role earn between $30.48 and $40.48 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 New Hope, MN are hiring for Clinical Data Associate jobs?

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

Clinical Data Associate jobs near you

Associate Clinical Data Manager

Abbott

Maple Grove, MN • On-site

Full-time

Medical, Retirement

Re-posted 15 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 122,000 colleagues serve people in more than 160 countries.

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, theFreedom 2 Save (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debtprogramandFreeU (https://www.abbott.com/corpnewsroom/strategy-and-strength/college-degree-for-free-its-possible-with-freeu.html) education 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. 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 ?nger sticks.

The Opportunity

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

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, incorporatingappropriatefeedbackandfinalizingtheCRF.?
  • Able to developspecifications fordata?listingsforcontinuous datareview,andcommunicate withdata analyticsteam membersthrough 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 thedata model.?
  • Able to develop edit check specifications toreviewfor illogical,?incomplete?and inconsistent data includingtesting and troubleshooting of?edits?checks.?
  • Identifies,?analyzes,?proposes?solutions,?and?effectively?resolves?complex?data/database structureissuesbyexercisingappropriatejudgmentandcollaboratingwiththeclinicalprojectteammembersandothersharedservice?functions.
  • Contributes?to?the?development?and?maintenance?ofClinicalDatabasesystems,includingEDC,EditChecks,Reporting,Study?Notifications,?etc.?through?the?following:?
  • Partner?closely?with?Data Review?Management,StudyDatabaseManager, andDataAnalytics andSystemsand other Data Review team members.??
  • Perform?and?document?functional?and/or?user?acceptance?testing?on?study?databases,?reports,studynotifications,?and?database?customizations.
  • Utilize?existing?tools/reports,SQL,anddatabaseUItoidentifydataissuesanddriveresolutionswiththe?ClinicalStudyTeaminatimelymanner.?
  • Attend?ClinicalStudyTeammeetings.
  • Contribute technical?expertise?to cross functional teams through CRF changes and the impact on databases and propose implementation strategies.??
  • Assists?in?FDA?and?QualitySystem?audits?that?involve?ClinicalDatabase?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 forBiometrics.?
  • Contribute to?data?review?meetings?with?the?ClinicalStudyTeamandBiometricstoidentifydatacleaningissues?and?strategize?cleaning?efforts.
  • Monitoroveralldatamanagementtaskstoensurethattimelinesaremetandthatanyissuesareproactivelyidentifiedandresolved.?

Perform?other?duties?as?assigned.?

Required Qualifications

  • 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.

Preferred ? Qualifications

  • Bachelor'sdegree inbusiness administration, datascience,statisticsor life sciences.
  • 3years' experience inclinical operations or healthcare relatedfield.
  • Knowledge?of?data?management?practices?from?CRF?design?to?database?development?and?study?closure.??
  • Experience?with?using?ElectronicData Capture(EDC)?databasesandadvancedskill levelworking inExcel.
  • Knowledge of documentation practices in-line with?GoodClinicalDataManagementPractices,andotherFDAregulations?and?guidelines?is?required.??
  • Ability?to?leverage?and/or?engage?others?to?accomplish?projects.?
  • Solid?oral?and?written?communication?skills?and?analytical/problem-solvingskills.??
  • Mustbeabletoeffectivelymanagemultipleprojectsandtimelines.
  • Requires?the?ability?to?sit?or?stand?while?working?ona?computer?for?a?long?period?of?time.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx)

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews. Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

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.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email corpjat@abbott.com

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