Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information.
The scope of responsibilities will include:
- Maintenance of databases and tracking systems
- Serves as the primary sites contact point for vendors study supplies and access management
- Work with large amount of documents including their compiling procurement processing and filing
- Communication with company departments and external parties
- Communication point for investigative sites participating in the clinical research projects
- Coordination of sitespecific query resolution project training and access to vendorrelated systems for site teams
- Ensures proper administration of sites and vendors payments
- Receiving and routing all mails and incoming calls
- Assistance with meeting arrangements
- Preparation of draft agendas and minutes of project meetings
Qualifications :
- College/University Degree (Life Sciences)
- Prior administrative experience in Clinical Research / CRO environment preferably in an international setting
- Good organizational and planning skills problemsolving abilities flexibility
- Detailoriented able to multitask and work effectively in a fastpaced environment
- Teamoriented with excellent customer service and interpersonal skills including a positive attitude to tasks and projects
Remote Work :
No
Employment Type :
Fulltime