Clinical Data Abstractor
Chicago, IL · On-site
This position is responsible for abstracting key clinical data from electronic health records, preparing standardized case documentation, maintaining laboratory databases, ensuring required ...
Chicago, IL · On-site
This position is responsible for abstracting key clinical data from electronic health records, preparing standardized case documentation, maintaining laboratory databases, ensuring required ...
Chicago, IL · On-site
This position is responsible for abstracting key clinical data from electronic health records, preparing standardized case documentation, maintaining laboratory databases, ensuring required ...
San Diego, CA · On-site
$75K - $90K/yr
The Clinical Data Associate will contribute to the performance of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, and Standard ...
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San Diego, CA · On-site
$75K - $90K/yr
The Clinical Data Associate will contribute to the performance of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, and Standard ...
San Diego, CA · On-site
$75K - $90K/yr
The Clinical Data Associate will contribute to the performance of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, and Standard ...
San Diego, CA · On-site
$75K - $90K/yr
The Clinical Data Associate will contribute to the performance of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, and Standard ...
Atlanta, GA · On-site
$23.25 - $31/hr
Maintain data standards, ontologies, and metadata frameworks in alignment with best practices and regulatory requirements. Ensure adherence to clinical trial regulatory requirements (IRB, HIPAA, GCP ...
Atlanta, GA · On-site
$23.25 - $31/hr
Maintain data standards, ontologies, and metadata frameworks in alignment with best practices and regulatory requirements. Ensure adherence to clinical trial regulatory requirements (IRB, HIPAA, GCP ...
Chicago, IL · On-site
$50K - $70K/yr
This position is responsible for abstracting key clinical data from electronic health records, preparing standardized case documentation, maintaining laboratory databases, ensuring required ...
Chicago, IL · On-site
$50K - $70K/yr
This position is responsible for abstracting key clinical data from electronic health records, preparing standardized case documentation, maintaining laboratory databases, ensuring required ...
Austin, TX · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance ... As a Clinical Data Coordinator, you will perform all aspects of the data cleaning process, with ...
Austin, TX · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance ... As a Clinical Data Coordinator, you will perform all aspects of the data cleaning process, with ...
Pittsburgh, PA · Hybrid
The Clinical Data Manager develops and manages the data spec development during the implementation ... Adheres to current accreditation standards and assists in the execution of updates to these ...
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Pittsburgh, PA · Hybrid
The Clinical Data Manager develops and manages the data spec development during the implementation ... Adheres to current accreditation standards and assists in the execution of updates to these ...
... data standards. Depending on organizational needs, interns may be assigned to: * Clinical Trial ... Start-up * Clinical Trial Execution * Clinical Trial Lock * Automation/Innovation projects Lilly ...
... data standards. Depending on organizational needs, interns may be assigned to: * Clinical Trial ... Start-up * Clinical Trial Execution * Clinical Trial Lock * Automation/Innovation projects Lilly ...
Knowledge of industry standards and practices. * Aware of the clinical development process ... data management experience. Additional Information For more information, please contact Sneha ...
Knowledge of industry standards and practices. * Aware of the clinical development process ... data management experience. Additional Information For more information, please contact Sneha ...
The candidate will own data across various studies, trace anomalies to their root causes, and maintain compliance with FDA standards. The role requires over three years of experience in clinical data ...
The candidate will own data across various studies, trace anomalies to their root causes, and maintain compliance with FDA standards. The role requires over three years of experience in clinical data ...
... standards. Review and contribute to the development of trial validation plan related documents and ... Support and assist clinical data managers, clinical data assistants for allocated trials. All other ...
... standards. Review and contribute to the development of trial validation plan related documents and ... Support and assist clinical data managers, clinical data assistants for allocated trials. All other ...
The candidate will own data across various studies, trace anomalies to their root causes, and maintain compliance with FDA standards. The role requires over three years of experience in clinical data ...
The candidate will own data across various studies, trace anomalies to their root causes, and maintain compliance with FDA standards. The role requires over three years of experience in clinical data ...
Irvine, CA · On-site
Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of ... flowcharts, Standard Operating Procedures (SOP), work instructions, training guidelines, etc.
Irvine, CA · On-site
Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of ... flowcharts, Standard Operating Procedures (SOP), work instructions, training guidelines, etc.
Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures. * Contribute to the maintenance of GCA's data ...
Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures. * Contribute to the maintenance of GCA's data ...
Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures. * Contribute to the maintenance of GCA's data ...
Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures. * Contribute to the maintenance of GCA's data ...
Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures. * Contribute to the maintenance of GCA's data ...
Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures. * Contribute to the maintenance of GCA's data ...
We're looking for someone who can manage their own work, believes in careful attention to standards ... clinical data. * Ability to work independently and balance competing priorities and complex ...
We're looking for someone who can manage their own work, believes in careful attention to standards ... clinical data. * Ability to work independently and balance competing priorities and complex ...
Phoenix, AZ · On-site
Maintains established productivity standards * Maintains competency in measure and/or registry ... to clinical data abstractor lead and/or director in a timely manner. * Established effective ...
Phoenix, AZ · On-site
Maintains established productivity standards * Maintains competency in measure and/or registry ... to clinical data abstractor lead and/or director in a timely manner. * Established effective ...
Phoenix, AZ · On-site
Maintains established productivity standards * Maintains competency in measure and/or registry ... to clinical data abstractor lead and/or director in a timely manner. * Established effective ...
Phoenix, AZ · On-site
Maintains established productivity standards * Maintains competency in measure and/or registry ... to clinical data abstractor lead and/or director in a timely manner. * Established effective ...
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Full-time
Re-posted 10 hours ago
Under general supervision of the Director of Laboratory Operations and in collaboration with the Analysis and Reporting team, the Clinical Data Abstractor will support the clinical laboratory by reviewing patient medical records, organizing clinical information, and preparing cases for downstream analysis including post-accessioning second review. This position is responsible for abstracting key clinical data from electronic health records, preparing standardized case documentation, maintaining laboratory databases, ensuring required documentation is complete, and supporting laboratory workflows through administrative and operational activities. The Clinical Data Abstractor will work closely with Clinical Genomic Analysts/Scientists and laboratory personnel to promote accurate, efficient, and timely patient reporting.Must be eligible to work in the United States.
Responsibilities:
Education and Experience Qualifications:
Required knowledge: