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Regulatory & Start-up Clinical Trial Assistant
il y a 2 semaines
The IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. The Global Site Activation team will help them to decrease the site activation time and help the site to be ready to recruit patients faster. We seek dynamic and motivated people who truly want to make a difference in the life sciences industry. At IQVIA, we look for the very best people and give them meaningful work to do. We don’t simply think about careers, we think about contributions.
The RSU CTA will have the following responsibilities:
- Assist the clinical team and the sites with the preparation, handling, distribution of clinical documentation and reports according to the scope of work and standard operating procedures,
- Assist CRAs, RSU specialists, vendors with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information,
- Assist CRAs in the Site Initiation visit with the preparation and the distribution of the Investigator and Pharmacy Site binders,
- Assist CRAs at the Site Activation with the site documents recovery.
The RSU CTA has:
- High or secondary school diploma/certificate or country’s educational equivalent and 2 years administrative support experience,
- Basic knowledge of applicable clinical research regulatory requirements preferred,
- Effective written and verbal communication skills of English and French languages,
- Computer skills including working knowledge of Microsoft Word, Excel and Outlook,
- Effective time management and organizational skills,
- Ability to establish and maintain effective working relationships with coworkers, managers and customers.
The position is located in France, office-based in La Défense.
LI-MP4
