LAS Operations Training Specialist

Abbott; Madison (WI); On-site; USD 61,000 - 123,000; Full time

Job summary

Abbott in Madison, WI is seeking an individual contributor who will work under limited supervision to manage clinical data. The role requires applying subject matter knowledge to understand specific study needs and ensure accurate data handling across therapeutic groups.

You will process and review patient data, support data management plans, comply with GCP guidelines, and collaborate with the medical department.

Qualifications

• Associate's degree in a related field.
• Minimum 1 year of experience in data management.
• Knowledge of drug and disease terminology.
• Understanding Good Clinical Practices (GCP) data handling.

Responsibilities

• Processes, reviews, and receives patient data and records and organizes clinical data forms.
• 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.
• 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.

Skills

Data management

GCP knowledge

Clinical data

Data validation

Education

Associate's degree

Job description

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-handing 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.