Site Management Associate

Start your career in clinical research streamlining communication maintaining systems and managing documents.

The scope of responsibilities will include:

• Maintenance of databases and tracking systems
• Work with large amount of documents including their compiling procurement processing translation and filing
• Communication with company departments and external parties
• Communication point for investigative sites participating in the clinical research projects
• Coordination of site-specific query resolution project training and access to vendor-related systems for site teams
• Receiving and routing all mails and incoming calls
• Assistance with meeting arrangements
• Preparation of draft agendas and minutes of project meetings

Qualifications :

• At least 6 months of experience in administrative and documentation management within clinical research
• Life Sciences university degree
• Full professional working proficiency in Dutch and English
• Good organizational and planning skills
• Detail-oriented able to multi-task and work effectively in a fast-paced environment
• Good problem-solving abilities flexibility
• Team-oriented with excellent customer service and interpersonal skills including a positive attitude to tasks and projects
• Proficiency in standard MS Office applications (Word Excel and PowerPoint)

Additional Information :

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Remote Work :

Yes

Employment Type :

Full-time