LAS Operations Training Specialist

RXinsider LTD.; Madison, Northern (WI, KY); Hybrid; USD 61,000 - 123,000; Full time

Job summary

Abbott is a global healthcare leader with a broad portfolio spanning diagnostics, medical devices, nutritionals and branded medicines. This role focuses on handling patient data, ensuring data quality, and supporting clinical research activities.

You will work under limited supervision as an individual contributor, applying subject matter knowledge to understand and meet specific needs within clinical data management and regulatory guidelines.

Qualifications

• Education Level Major/Field of Study or Equivalent
• Associate's degree (± 13 years)
• Language Proficiency

Responsibilities

• Processes, reviews, and receives patient data and records and organizes clinical data forms from particular therapeutic groups and outside investigators.
• Provides accurate, timely, and consistent clinical data to the medical department and other groups.
• Responsible for data management plans including data preparation, data validation activities, etc.
• Follows Good Clinical Practices (GCP) data-handling procedures and guidelines.
• Requires knowledge of drug and disease terminology.
• May manage service providers that perform these activities.
• Participates in the review of clinical research protocols, reports and statistical analysis plans.

Education

Associate's degree (± 13 years)

Job description

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, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

MAIN PURPOSE OF THE ROLE

Individual contributor that works under limited supervision.

Applies subject matter knowledge.

Requires capacity to understand specific needs or requirements to apply skills/knowledge.

Main Responsibilities

• Processes, reviews, and receives patient data and records and organizes clinical data forms from particular therapeutic groups and outside investigators.


• Provides accurate, timely, and consistent clinical data to the medical department and other groups.


• Responsible for data management plans including data preparation, data validation activities, etc.


• Follows Good Clinical Practices (GCP) data-handling procedures and guidelines.


• Requires knowledge of drug and disease terminology.


• May manage service providers that perform these activities.


• Participates in the review of clinical research protocols, reports and statistical analysis plans.

Qualifications

Education

Education Level Major/Field of Study or Equivalent

Associate's degree (± 13 years)

Experience/Background

Experience Details

Minimum 1 year

Licenses and Certifications

Language Proficiency

Language

The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted.