Clinical Data Manager

Abbott; Maple Grove (MN); On-site; USD 55,104 - 82,656; Full time

Benefits offered by this job

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

Health Savings Account

Flexible Spending Accounts (Health, LD

Flexible Spending Accounts (Dependent)

Supplemental Life Insurance

Short Term Disability

Long Term Disability

Critical Illness, Hospital coverage, /

MetLife Legal, MetLife ID Fraud, and/

401(k)

Job summary

Abbott is seeking a Clinical Data Manager for a 7‑month, 100% onsite engagement in Maple Grove, MN. The role centers on managing risk-based quality management systems, data reviews, and cross‑functional collaboration with therapy groups to align data interpretation with study requirements.

You will lead risk identification and mitigation, oversee data cleaning, and coordinate with stakeholders to resolve data quality issues and ensure study integrity across sites.

Qualifications

• 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 identifying risks in a process, evaluating likelihood and impact, and developing mitigation/monitoring strategies.

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.

Skills

Risk assessment

Data management

Clinical operations

Project management

Life sciences

Communication

Education

Bachelor's Degree (± 16 years)

Biology, Health Sciences, Mathematics, Computer Science or equivalent

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)