Job Description

Our client are looking for an Administrator, if you're looking for a busy and challenging role working for a company that takes pride in looking after their employees - then please apply!

Responsibilities:

• Organise, maintain and complete the paper and electronic trial master files, including collation of study documents from monitors or CROs and appropriate filing of documents.
• Identify, request and ensure delivery of outstanding and outdated documents.
• Periodically, and at the end of the study, review study files / folders for organization and completeness.
• Assist in setting up clinical study files / folders at study sites and assist in quality review of the study site files / folders throughout the study.
• Assist the COPMs by offering support for day-to-day study management activities, to include:
• Tracking the distribution of protocols and protocol amendments.
• Creating drafts of study-specific documents.
• Seeking signatures for approved documents.
• Conduct in-house clinical operations functions, including clinical supplies coordination, , Assist the COPM in investigator meeting preparation and coordination, document processing and study status tracking.
• Arranging and minuting Study Team Meetings (as required) and completing actions as necessary.
• Assist in the project management and monitoring of clinical studies, including liaison with study sites, monitors, CROs, drug vendors, central laboratories and other vendors for study related tasks.
• Perform various study related functions as required and assigned to ensure the accurate, quality, timely and on budget execution of clinical studies, to include:
• Maintaining budget tracking tools as appropriate.
• To perform any other activity as may reasonably be required from time to time.

Required Knowledge, Skills, and Abilities