This position is open at our office in Copenhagen, Denmark.

LINK Medical Research is searching for a highly motivated fulltime CRA at our office in Copenhagen, Denmark. As a CRA, you will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas. You may also be outsourced to clients in the greater Copenhagen area and the position will involve frequent travelling related to monitoring visits.

Responsibilities

· Plan and perform site feasibility, initiation, monitoring, and close-out activities in accordance with the protocol, ICH-GCP, applicable regulations, monitoring plans, and SOPs

· Perform Source Data Verification (SDV) and review of Case Report Forms (CRFs)

· Preparation, handling and distribution of clinical study supplies and products when applicable

· Comply with applicable timelines, agreements and budget

· Maintain TMF completeness and inspection readiness and support trial supplies, informed consent materials, and regulatory submissions

· Assess and escalate study risks, issues, and deviations and provide transparent progress reporting

· Act as the main contact for assigned sites, support participant recruitment and retention, and train site staff

Desired qualifications

· Basic education within relevant field, equivalent to degree from University or University level. Formal education may be compensated by experience.

· Up to date on ICH-GCP including national regulatory requirements

· Experienced in monitoring studies or running clinical studies and in investigator site management

· Must be fluent in Danish (required) and English

· Good writing skills in both Danish and English

· Effective verbal and written communication

· Generally good IT skills and use of standard office tools

Personal Characteristics

· Service minded with good cooperation and communication skills, as well as oral and written presentation skills

· Well organized and structured, able to work both independently and in teams

· Independent, flexible, accurate, and solution oriented

LINK Medical offers

We offer an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our employees in an international environment and values as honest and open communication are essential. You will be given meaningful tasks requiring efficient collaboration between industry, clinical and scientific teams, and the authorities. Besides a great working environment with dedicated and supporting colleagues, we also offer a competitive compensation, benefit scheme and great development opportunities for all employees.

Contact Information

If you would like to know more or if you have any questions about the position, please contact Director of Clinical Operations Trine Dyring, +45 4127 8470, trine.dyring.jensen@linkmedical.eu

All applications are treated confidentially.
Last day for application: 30th of October 2026.