Join us as Senior Clinical Data Manager

Written By Signifikans

Come to Signifikans - well known for innovation and no bureaucracy, to take responsibility and perform all aspects of data management work for assigned studies/projects from multiple therapeutic areas.

We seek a skilled professional to:

•Serve as the main client contact for clinical data matters

•Set up and test databases in eCRF/ePRO systems

•Conduct risk-based data monitoring, dashboard analysis, and database lock

•Develop relevant documentation such as Data Management and Data Handling Plans

•Manage administrative tasks for Data Monitoring Committees (DMCs), including data presentations and meeting minutes

•Lead data handling project teams and coordinate with colleagues

•Maintain structured workflows and documentation

•Contribute to updating internal standards and SOPs

You are and have:

•Bachelors (minimum) in life science, statistics, computer science, or equivalent experience

•Minimum 3 years in drug development and clinical data handling

•Proficient in eCRF/ePRO systems and MS Office; basic SAS and SQL skills

•Strong knowledge of physiology, drug development, GCP, clinical trial methodology, medical terminology and CDASH standards

•Excellent organizational, project management, and problem-solving skills

•Effective communication and interpersonal skills for internal and external collaboration

•You thrive working Independent, structured, and flexible and like taking initiative

Working place: In our modern office in Vedbæk, partly work-from-home or remote is also possible.

You will receive:   

•A role in an innovative, entrepreneurial organization with no bureaucracy

•Access to cutting-edge technology to support your work and client success

•Influence over your daily work and processes

•Competitive salary, pension, health insurance, and performance-based annual bonus

Start: 1. May 2025.

Contact: Andreas Habicht at +45 23 70 84 22 and apply on mail to ah@signifikans.dk by 1 April 2026.

Signifikans