Abbott Laboratories Work Values

Daily Duties at Abbott Laboratories:

 Monitored several clinical sites in US for accuracy and data/document integrity throughout the course of a study by doing pre-qual, initiation, interim and close out visits, ensured smooth execution of design validation studies  Designed and reviewed case report forms and study packets for the clinical sites; authored basic protocols and clinical brochures in compliance with the Good Clinical Practice guidelines  Ensured that clinical investigative sites are protecting the subject’s rights and safety, adhering to clinical protocols, Standard Operating Procedures, ICH guidelines, Good Clinical Practices and FDA regulations and also the HIPPA Guidelines  Reviewed the investigational sites regulatory documents according to ICH/GCP guidelines and 21 CFR, IUO product accountability Forms, and prepared site visit reports  Audited multiple in-house specimen collection studies for accuracy and patient integrity to ensure compliance with Abbott Laboratories Standard Operating Procedures

What they like about Abbott Laboratories:

The social vibrance of a hiring firm is very important to you. Your ability to make and maintain friendships there is a critical part of your decision. You would likely be dissatisfied with a workplace that is quiet, cold, or otherwise not particularly social. When you investigate a new hiring company, ask recruiters, managers, and potential co-workers about the social life and opportunities there. This is especially important when you are relocating; moving dramatically alters your social sphere both inside and outside the workplace.

Tags

SANTA CLARA, SUNNYVALE, DIAGNOSTIC COMPANY, RESEARCH AND DEVELOPMENT , QUALITY, CLI SCRIPTING

Skills

 Trained in using the following Abbott Instruments: ARCHITECT immunoassay System (i1000SR and i2000SR instruments), ARCHITECT clinical chemistry System (C8000 and C4000 instruments),  Proficient in CLI scripting; authored Maintenance & Diagnostic procedures,  Familiar with conducting data analysis via JMP programming,  Working knowledge of extracting data from Abbott Link and using LOG-IC to run log analysis,  Knowledge of regulations and standards affecting IVDs and Biologics

These are some of the questions we asked our climbers about their experiences with Abbott Laboratories: