CTMS administrator

Responsibilities:
• Updating clinical trial systems and databases (CTMS) with operational data information
• Ensuring data is accurate and complete using different reports and applications
• Engaging with study leads (internal or external) and IT supporting functions (internal and external) to ensure data accuracy and completeness. Working in accordance to SOP and regulatory requirements
Requirements:
• Bachelor’s degree in life science
• +1.5Y Experience as clinical trials Assistant/administrator/coordinator
• Comfortable working in a technological environment (usage of share drives, SharePoint, CRM systems)
• Proficient in Excel, Word, Outlook
• English – Business-level proficiency (must be comfortable to engage with others in English on regular basis)
• High work ethics, Strong organizational skills, Attention to details
Additional experience – advantage:
• High- Prior work experience with CTMS system for trail oversight/management (Siebel Oracle)
• At least one year of experience as Clinical data manager
This position is a temporary position for a maternity leave replacement; open for men and women alike.
 
 
replacement for maternity leave
 
5 days a week
flexeabilty in work hours
can work remotly or in the site