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Clinical Data Jobs in Minnesota (NOW HIRING)

Clinical Data Translation: Translate complex trial data on devices used in cardiac ablation into clear scientific narratives. * Congress Strategy: Lead abstract submission strategies for major ...

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Clinical Data information

See Minnesota salary details

$19

$55

$80

How much do clinical data jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical data 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 is clinical data?

Clinical data refers to information collected during the course of ongoing patient care or as part of a clinical trial program. This data includes patient demographics, medical history, lab results, imaging studies, treatment plans, and outcomes. Clinical data is crucial for informing medical decisions, improving patient care, and supporting medical research and drug development. It is typically collected and managed by healthcare providers, researchers, and data professionals while maintaining strict standards for patient privacy and data security.

What are some common challenges faced by professionals working in clinical data roles, and how can they be addressed?

Professionals in Clinical Data roles often encounter challenges such as managing large volumes of complex data, ensuring data quality and integrity, and adhering to strict regulatory standards. These challenges can be addressed by staying updated on industry best practices, utilizing advanced data management tools, and working closely with cross-functional teams such as clinical research and regulatory affairs. Continuous professional development and effective communication within the team are also key to overcoming these hurdles and ensuring successful clinical trial outcomes.

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

To thrive as a Clinical Data Specialist, you need a solid background in life sciences, data management principles, and familiarity with regulatory guidelines, often supported by a relevant degree. Proficiency in clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of standards like CDISC or MedDRA is typically required. Strong attention to detail, analytical thinking, and effective communication skills are crucial soft skills for this role. These competencies ensure the accuracy and integrity of clinical trial data, supporting regulatory compliance and reliable outcomes in clinical research.

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

AspectClinical DataClinical Data Coordinator
CredentialsTypically requires a degree in health informatics, life sciences, or related fieldRequires similar credentials, often with additional certification in clinical research or data management
Work EnvironmentData analysis, database management, and reporting in healthcare or research settingsOversees data collection, entry, and quality control in clinical trial or healthcare environments
Employer & Industry UsageUsed across hospitals, research institutions, and pharmaceutical companiesCommonly employed in clinical research organizations and hospitals

While both roles involve handling clinical data, Clinical Data professionals focus on data analysis and management, whereas Clinical Data Coordinators oversee data collection and quality assurance in clinical trials or healthcare settings.

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

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

Infographic showing various Clinical Data job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 9% Part Time, and 6% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $116,461 per year, or $56 per hour.

Sr. Clinical Publication Manager

Abbott

Plymouth, MN • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 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:

Sr. Clinical Publication Manager

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your 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 a 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our St Paul or Plymouth, MN location for our Electrophysiology medical device business. In Abbott's Electrophysiology (EP) business, we're advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.

What You'll Work On

TheSr. Clinical Publication Manager in Electrophysiologydesigns and delivers the scientific publication plan for in-human electrophysiology device data. They lead a team of medical writers and work closely with cross-functional partners and external stakeholders to translate complex clinical trial findings into peer-reviewed manuscripts and congress presentations. The Clinical Publications Manager (Electrophysiology) will lead the strategic development and execution of global publication plans. This role will report through the Electrophysiology Clinical Affairs Department within Abbott Medical Devices - Electrophysiology business. This role ensures timely, ethical, and compliant publication of clinical data for our electrophysiology portfolio.

Specialized Electrophysiology Responsibilities

  • Clinical Data Translation:Translate complex trial data on devices used in cardiac ablation into clear scientific narratives.

  • Congress Strategy:Lead abstract submission strategies for major cardiology congresses like the Heart Rhythm Society (HRS) and European Heart Rhythm Association (EHRA).

  • Stakeholder Management:Partner directly with electrophysiologists, cardiac surgeons, and trial investigators to co-author manuscripts.

  • Device Safety Reporting:Manage publication timelines for post-market clinical follow-up (PMCF) studies and registry data.

Strategic Publication Planning

  • Develop annual publication plans for electrophysiology assets.

  • Align publication timing with product launch milestones.

  • Manage timelines for data disclosure.

  • Collaborate closely with cross-functional partners in R&D, marketing, medical affairs, and Biometrics.

Content Generation & Oversight

  • Coordinate writing of abstracts and manuscripts and development of posters and podium presentations.

  • Review technical documents for clinical accuracy.

  • Manage external medical communication agency partners.

Compliance & Integrity

  • Enforce Good Publication Practice (GPP) standards.

  • Follow International Committee of Medical Journal Editors (ICMJE) guidelines.

  • Maintain documentation in publication management databases.

Required Qualifications

  • Education:Advanced scientific degree (PhD, PharmD, MD, or Master's in bioengineering/life sciences).

  • Experience:5-7+ years in medical publications or medical communications.

  • Domain Expertise:Strong background in cardiology, medical devices, or cardiac electrophysiology.

  • Skills:Expert knowledge of clinical trial designs and statistical methodologies.

What We Offer

At Abbott, you can have a good job that can grow into a great career. We offer:

  • A fast-paced work environment where your safety is our priority

  • Production areas that are clean, well-lit and temperature-controlled

  • Training and career development, with onboarding programs for new employees and tuition assistance

  • Financial security through competitive compensation, incentives and retirement plans

  • Health care and well-being programs including medical, dental, vision, wellness and occupational health programs

  • Paid time off

  • 401(k) retirement savings with a generous company match

  • The stability of a company with a record of strong financial performance and history of being actively involved in local communities

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

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 X @AbbottNews.

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:Clinical Affairs / StatisticsDIVISION:EP ElectrophysiologyLOCATION:United States > Minnesota > St. Paul > Lillehei : One Lillehei PlazaADDITIONAL LOCATIONS:United States > Minnesota > Plymouth : 5050 Nathan Lane NWORK 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

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