Description
We are seeking a Clinical Research Coordinator to perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
The successful candidate will work under general supervision to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary.
Responsibilities include:
- Reviewing documents for completeness, consistency and accuracy
- Preparing site documents, reviewing for completeness and accuracy
- Informing team members of completion of regulatory, contractual and other documents for individual sites
- Distributing completed documents to sites and internal project team members
- Supporting the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information
- Reviewing, tracking and following up the progress, the approval and execution of required documents
Requirements:
- Bachelor's Degree in Life science or related field
- 2 years' experience in a clinical research environment
- Fluency in both Dutch and French
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.