Clinical Operations Specialist (Hybrid, Denmark)

Job summary

The role involves supporting clinical operations by ensuring compliance with corporate policies and assisting with site management activities. The specialist will act as a representative for assigned studies and maintain essential documentation.

Qualifications

• High School diploma or equivalent
• Strong communication and interpersonal skills
• Willingness to adopt new technologies
• Minimal travel up to 25% may be required

Responsibilities

• Perform activities in line with Corporate and Clinical Operations Policies and Standard Operating Procedures
• Assist Clinical Monitoring staff with site management and compliance communication
• Create and maintain Trial Master File (TMF) and project files, participating in audits
• Prepare and maintain site manuals and reference documents
• Update and input clinical tracking information into databases
• Manage incoming and outgoing clinical and regulatory documents
• Coordinate the ordering and tracking of site supplies
• Assist with team meeting coordination and documentation
• Handle receipt and tracking of Case Report Forms and Queries
• Stay informed on clinical research through assigned training

Skills

• Good communication and interpersonal skills
• Ability to embrace new technologies

Education

• High School diploma or equivalent

Tools

• Clinical tracking databases