Clinical Process Compliance Associate (Hybrid)
AbbVie
Full-time
Remote friendly (Florham Park, NJ)
United States
$64,000 - $122,000 USD yearly
Clinical Research and Development
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Role Summary
Clinical Process Compliance Associate (Hybrid) – Independent contributor supporting Quality Control, Compliance, and/or Metrics to oversee clinical trial activities in alignment with GCP and AbbVie procedures.
Responsibilities
- Responsible for compliance with applicable Corporate and Divisional policies and procedures.
- Assist in the completion of activities regarding quality control, compliance, investigational product release for clinical studies and/or data collection; collaborate with functional areas to ensure activities are completed per plan.
- Communicate clinical-related information and escalate issues to management with possible resolutions.
- Maintain SharePoint and other systems required to support functional activities.
Qualifications
- Bachelor’s degree (or equivalent ex-US) required, typically in nursing or scientific field; an Associate’s degree/R.N. (or equivalent ex-US) with relevant experience is acceptable.
- 2+ years Pharma-related/clinical research experience.
- Experience applying standard business procedures (SOPs, ICH, Global Regulations, Ethics and Compliance).
- Preferred: Quality certification.
Skills
- Demonstrates analytical and critical thinking skills.
- Good communication skills.