Clinical QC Compliance Associate III

«out AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Description – Clinical QC Compliance Associate III Overview: Position is required to be on-site 3-4 days a week. Responsible for compliance with applicable Corporate and Divisional policies and procedures. Perform QC review of CPPM regulatory, scientific and clinical documents. Lead project activities to ensure CPPM compliance to regulatory and corporate standards, including quality updates to standard documents and process enhancements across all CPPM. Identify issues that potentially impact study data, ethical study conduct, and global regulatory and AbbVie compliance and identify potential interventions or solutions to manage the issues. Provide valuable Quality Control and compliance support for internal audits and regulatory authority inspections of CPPM and ACPRU. Qualifications Qualifications: Bachelor’s degree (or equivalent ex-US) is required, typically in scientific field. An Associate’s degree/R.N. (or equivalent ex-US) with relevant experience is acceptable. Must have 4+ years of Pharma-related/ clinical research related experience. Must have demonstrated a high level of core and technical competencies. Possesses good communication skills. Competent in application of standard business procedures (SOPs, ICH, Global Regulations, Ethics and Compliance). Preferred exposure to clinical research from study initiation through study completion. Preferred experience with attaché, SumTotal, SolTRAQs, Vault. Significant Work Activities Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.