Parexel are currently recruiting for an experienced Clinical Trial Associate/Administrator to support a large global cardiology study.

In this position you will be an invaluable resource, providing support to the wider clinical study teams, helping to maintain system accuracy and ensuring on time delivery of clinical trial deliverables

Some Specifics About This Advertised Role

• Assist with the in-house coordination of activities related to the conduct of clinical trials
• Track progress across multiple programs and communicate this to internal and external stakeholders
• Assist in maintaining clinical invoice tracking and other budget databases for multiple projects; generate periodic reports on status of payments and other database reports, and resolve payment inquiries from investigator sites
• Maintain informational databases for clinical trial status throughout the life of a clinical program
• Responsible for the assembly, review, quality control, and tracking of regulatory documents
• Perform maintenance and tracking of study materials including investigational drug
• Organize trial and program related team meetings, associated agendas, and generate meeting minutes, including tracking of action items
  
  

• BS/ BA degree is preferred.
• Minimum 1+ years of clinical research experience gained with a CRO, Biotech or Pharmaceutical Company working on Phase 1-4 clinical trials.
• Experience supporting global/regional trials is essential