Drive clinical excellence as a Clinical Research Associate II at AbbVie. This role emphasizes the oversight of clinical site operations to ensure studies meet strict protocol standards.
Dedicated to transforming lives, AbbVie is seeking a skilled with two years of monitoring experience to enhance our R&D; capabilities. You will be responsible for conducting training, managing site compliance, and safeguarding the quality of data collected throughout clinical trials.
Key Responsibilities: • Monitor clinical study execution for protocol adherence • Facilitate site initiation and closeout processes • Engage site personnel to meet research goals • Ensure updated safety reporting and compliance • Train sites on regulatory requirements and protocols
Requirements: • Minimum of 2 years clinical monitoring experience • Proficient in ICH guidelines and GCPs • Strong organizational capabilities • Mastery of Microsoft Office tools • Valid driver's license and passport needed
Capitalize on your clinical expertise to support AbbVie in delivering innovative medical solutions to patients. #J-18808-Ljbffr
📌 Clinical Research Associate II Position (Winnipeg)
🏢 Allergan
📍 Winnipeg
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