Om tjänsten
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
- Maintain TMF completeness and inspection readiness and support trial supplies, informed consent materials, and regulatory
submissions
Desired qualifications
- Basic education within relevant field, equivalent to degree from University or University level. Formal education may be
compensated by experience.
Personal Characteristics
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.