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 – $122,700.00In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf