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Volunteer Clinical Data Manager Jobs (NOW HIRING)

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 ...

As our next Clinical Data Manager, you will have the opportunity to work closely with the multidisciplinary project team across the life cycle of the project to ensure data management is thoughtfully ...

New

Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of Extension) Employment Type: W2 Contingent Worker SUMMARY OF POSITION: As a key member of the Global ...

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, external partners, and vendors to design, configure, and test clinical database systems, conduct data ...

The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data ...

ZS is seeking a Tech Project Delivery Manager to lead a high-velocity team focused on the future of Biometrics and Clinical Data. We are looking for a delivery leader who excels at navigating the ...

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, external partners, and vendors to design, configure, and test clinical database systems, conduct data ...

The Senior Clinical Data Manager will be responsible for the oversight, coordination, and execution of clinical data management activities across one or more clinical trials. This individual will ...

Clinical Data Manager

New York, NY · On-site

$115K - $145K/yr

About the Role We are looking for a Clinical Data Manager to accelerate Novellia's data curation and delivery processes. In this role, you will be responsible for working with a team of cross ...

Overview Principal Clinical Data Manager Location: Remote About This Opportunity: This is an evergreen position intended to help us identify and engage with talented professionals for potential ...

About the Role We are looking for a Clinical Data Manager to accelerate Novellia's data curation and delivery processes. In this role, you will be responsible for working with a team of cross ...

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Volunteer Clinical Data Manager information

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How much do volunteer clinical data manager jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for volunteer clinical data manager in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What are popular job titles related to Volunteer Clinical Data Manager jobs?

For Volunteer Clinical Data Manager jobs, the most frequently searched job titles are:

Infographic showing various Volunteer Clinical Data Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $118,909 per year, or $57.2 per hour.

Clinical Data Manager

Maple Grove, MN • On-site

$45 - $47/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 27 days ago


Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 139 frontline employees who took The Breakroom Quiz


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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