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Clinical Data Monitor Jobs (NOW HIRING)

Abbott

Clinical Data Manager

Maple Grove, MN · On-site

$45 - $47/hr

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The ... Conduct Central Monitoring activities, as described in Central Monitoring Plan. * Direct all data ...

Viking Therapeutics

Clinical Data Manager

San Diego, CA · On-site

$110K - $120K/yr

The Clinical Data Manager will ensure timely conduct of Clinical Data Management activities for ... Monitor and contribute to data review processes to verify that timely and proficient data review is ...

University of Utah

Clinical Data Managers

Campus, IL · On-site

$39K - $54K/yr

Develop data management reports and monitor study status to ensure timelines are met. Represent the ... Work collaboratively with clinical research and operations team to ensure accurate and complete ...

University of Utah

Clinical Data Managers

Campus, IL · On-site

$39K - $54K/yr

Develop data management reports and monitor study status to ensure timelines are met. Represent the ... Work collaboratively with clinical research and operations team to ensure accurate and complete ...

University of Utah

Clinical Data Managers

Campus, IL

$39K - $54K/yr

Develop data management reports and monitor study status to ensure timelines are met. Represent the ... Work collaboratively with clinical research and operations team to ensure accurate and complete ...

Faeth Therapeutics

Clinical Data Manager

Austin, TX · On-site

$125K - $175K/yr

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M ... Monitor query generation and resolution timelines * Perform data review, listings review, and ...

Viltis

Be Seen First

Associate Clinical Data Manager

Maple Grove, MN · On-site

$40 - $50/hr

Monitor the overall health of clinical study data quality and study conduct throughout key milestones and deliverables. Required Qualifications * Bachelor's degree in Biology, Health Sciences ...

New

Faeth Therapeutics

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M ... Monitor query generation and resolution timelines * Perform data review, listings review, and ...

Viltis

Be Seen First

Associate Clinical Data Manager

Maple Grove, MN · On-site

$40 - $50/hr

Monitor the overall health of clinical study data quality and study conduct throughout key milestones and deliverables. Required Qualifications * Bachelor's degree in Biology, Health Sciences ...

New

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams ... Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project ...

Cynet Systems

Clinical Data Manager

Maple Grove, MN · On-site

$41.42 - $46.42/hr

Conduct Central Monitoring activities, as described in Central Monitoring Plan. * Direct all data cleaning activity related to assigned studies. Skills: * Clinical Science. * Biometrics. * Safety.

New

CYNET SYSTEMS

Clinical Data Manager

Maple Grove, MN · On-site

$41 - $46/hr

Conduct Central Monitoring activities, as described in Central Monitoring Plan. * Direct all data cleaning activity related to assigned studies. Skills: * Clinical Science. * Biometrics. * Safety.

New

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Clinical Data Monitor information

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How much do clinical data monitor jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical data monitor in the United States is $38.49, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $51.20 per hour, depending on experience, location, and employer.

What is a clinical data monitor?

A Clinical Data Monitor is a professional responsible for overseeing the accuracy, integrity, and security of data collected during clinical trials. They ensure that clinical trial data is collected, entered, and reported according to regulatory standards and study protocols. Their work helps maintain the quality of data used to assess the safety and effectiveness of new drugs or medical devices. Clinical Data Monitors often collaborate with clinical research coordinators, data managers, and regulatory authorities to ensure compliance and resolve any data discrepancies.

How does a clinical data monitor typically interact with other teams during a clinical trial?

Clinical Data Monitors work closely with various teams such as clinical research associates (CRAs), data management, and biostatistics. They are responsible for ensuring the accuracy and integrity of clinical trial data by regularly reviewing case report forms and addressing discrepancies with site staff and data managers. Effective communication and collaboration are crucial, as Clinical Data Monitors often need to provide feedback, clarify data inconsistencies, and ensure all regulatory and protocol requirements are met throughout the trial.

How to become a clinical data monitor?

To become a clinical data monitor, typically a bachelor's degree in health sciences, life sciences, or a related field is required. Relevant skills include knowledge of clinical trial processes, data management, and familiarity with electronic data capture systems; obtaining certifications like the Society of Clinical Data Management (SCDM) certification can enhance prospects. Gaining experience through internships or entry-level roles in clinical research is also beneficial.

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

To thrive as a Clinical Data Monitor, you need a solid understanding of clinical research processes, data management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of Good Clinical Practice (GCP) guidelines are typically required. Attention to detail, analytical thinking, and strong communication skills set outstanding professionals apart in this role. These skills are crucial to ensure the accuracy, integrity, and regulatory compliance of clinical trial data, which supports successful drug development and patient safety.

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

AspectClinical Data MonitorClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or healthcare, often with certifications like CDMP or CDISCUsually holds a degree in health sciences or related field, with similar certifications
Work EnvironmentWorks primarily on data review, monitoring clinical trial sites, and ensuring data qualityHandles data entry, management, and coordination between sites and sponsors
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, hospitals, clinical trial sites

The Clinical Data Monitor focuses on reviewing and verifying clinical trial data to ensure accuracy and compliance, often working directly with sites. The Clinical Data Coordinator manages data entry and organization, supporting the data collection process. Both roles require similar educational backgrounds and certifications but differ in daily responsibilities and focus areas.

More about Clinical Data Monitor jobs
What states have the most Clinical Data Monitor jobs? States with the most job openings for Clinical Data Monitor jobs include:
What job categories do people searching Clinical Data Monitor jobs look for? The top searched job categories for Clinical Data Monitor jobs are:
Clinical Data Monitor jobs near you
Infographic showing various Clinical Data Monitor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $80,060 per year, or $38.5 per hour.

Clinical Data Manager

Abbott

Maple Grove, MN • On-site

$45 - $47/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 26 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

178th of 538 rated manufacturers

Job description

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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