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Clinical Data Associate Per Diem Jobs in Minnesota

A24Group

Per Diem Registered Nurse

Minneapolis, MN · On-site

$46.20 - $53.90/hr

Strong clinical judgment and communication skills Additional Details * Per diem flexibility * Must bring valid government-issued ID * Facility compliance requirements apply

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 ...

A24Group

Per Diem Registered Nurse

Minneapolis, MN · On-site

$50.40 - $58.80/hr

Strong critical thinking and clinical skills Additional Details * Per diem flexibility * Must bring valid government-issued ID * Facility compliance requirements apply

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Clinical Data Associate Per Diem information

What is the difference between Clinical Data Associate Per Diem vs Clinical Data Coordinator?

AspectClinical Data Associate Per DiemClinical Data Coordinator
CertificationsTypically requires a degree in life sciences or related field; certifications like CDISC or CDMP are a plusSimilar certification requirements; often holds additional project management or data management certifications
Work EnvironmentTemporary, flexible schedules; often in clinical research settingsFull-time, permanent roles; involved in ongoing data management projects
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for short-term data tasksEmployed by similar organizations for overseeing data integrity and compliance

The main difference is that Clinical Data Associate Per Diem roles are temporary and flexible, focusing on specific data tasks, while Clinical Data Coordinators hold permanent positions with broader responsibilities in managing clinical data processes.

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Clinical Data Associate Per Diem jobs near you

Associate Clinical Data Manager

Siro Clinpharm Pvt Ltd

Maple Grove, MN • On-site

Other

Posted 3 days ago

New

Job description

Associate Clinical Data Manager
Location : Maple Grove, MNRole Summary

The Associate Clinical Data Manager supports the planning and execution of clinical study data management activities. Under the direction of a manager, this role leads cross-functional teams through case report form development, database setup, data review, and data cleaning processes to ensure the integrity and quality of clinical study data throughout the lifecycle of an investigation.

Key Responsibilities

• Leads cross-functional teams during protocol development to identify and document data critical to the reliability of

study results and protection of human subjects.

• Manages the development and revision of case report forms (CRF), edit checks, data listings, and clinical

database setup.

• Identifies and evaluates residual risks to critical study data; oversees development of additional mitigations

including focused data cleaning, quality activities, and targeted site instructions.

• Leads the Clinical Project Team through CRF development and partners with the Study Database Manager

through database development, release, programming, and testing of edit checks.

• Conducts review and analysis of subject data as it accumulates, resolving discrepant or aberrant data points via

queries to study sites.

• Identifies systemic or significant data quality issues requiring escalation; manages escalation in partnership with

Project Management, Site Management, Clinical Science, Biometrics, and Safety.

• Manages progress toward data cleaning and data freeze/lock targets for regulatory submission.

• Manages issuance and resolution of discrepancies over the study lifecycle, including root cause analysis and

development of system-level countermeasures and process improvements.

• Leads proactive partnership with field and study team personnel, presenting findings from central monitoring and

data review activities.

• Assists in ongoing risk evaluation through in-depth review of protocol and plan documentation, validation of risk

findings, and development of process-based controls.

• Contributes to the maintenance of data review standards and best practices.

Required Qualifications

• Bachelor’s degree in Biology, Health Sciences, Mathematics, Computer Science, or equivalent field.

• Minimum 5 years of experience in clinical operations or a healthcare-related field.

• Knowledge of Good Clinical Practice (Google Cloud Platform) and global regulations for investigational studies.

• Strong analytical and critical thinking skills with demonstrated data management experience.

• Strong written and verbal communication skills; ability to lead discussions and manage complex regulated studies.

• Ability to effectively influence cross-functional team decisions.

Preferred Qualifications

• Certified Clinical Data Manager (CCDM) designation.

 

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