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Site Management Associate

📅 Jun 25
📍 🇺🇸 Netherlands - Remote🪈 Entry-level🎲 Other📢 🇳🇱 Dutch Required📢 🇬🇧 English Required💼 Full-Time
Database ManagementDocumentation ManagementCommunication SkillsOrganizational Skills

📜 Description

  • Maintenance of databases and tracking systems
  • Work with large amounts of documents, including compiling, procurement, processing, translation, and filing
  • Communication with company departments and external parties
  • Serve as a communication point for investigative sites in clinical research projects
  • Coordinate site-specific query resolution, project training, and access to vendor-related systems
  • Assist with meeting arrangements and prepare draft agendas and minutes

🛠️ Requirements

  • 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)
Full job description

Company Description

We are the company that cares; for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

This remote position is open to candidates based anywhere in the Netherlands.

Job Description

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.

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