LAS Operations Training Specialist

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

Job summary

Abbott Laboratories is seeking a clinical data professional to work under limited supervision, applying subject matter knowledge to organize and manage patient data. This role requires understanding specific needs to apply data-handling skills and ensures accurate data transfer to the medical department.

The position focuses on data management plans, validation activities, and adherence to GCP guidelines while supporting review of clinical research protocols and statistical analysis plans.

Qualifications

• Associate's degree or equivalent required.
• Minimum 1 year of experience.
• Familiarity with clinical data forms and records.
• Knowledge of drug and disease terminology.

Responsibilities

• Process, review, and organize clinical data forms from therapeutic groups.
• Provide accurate, timely clinical data to the medical department and other groups.
• Manage data management plans including data preparation and validation activities.
• Follow Good Clinical Practices (GCP) data-handling procedures and guidelines.
• Participate in review of protocols, reports and statistical analysis plans.

Skills

Clinical data

Data validation

GCP guidelines

Medical terminology

Communication

Education

Associate degree

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.