(Sr) Clinical Research Associate

As LINK Medical continues to grow, we currently have an open (Sr) CRA position at our office in Berlin (DE), with potential opportunities arising at our other offices (SE, NO, FI, DK and UK).

With 30 years in the industry and around 150 highly qualified and experienced colleagues, we pride ourselves on having the best full-service CRO and Regulatory team in the Nordic region offering a wide range of expertise, flexible services for the pharmaceutical and medical device industries

LINK Medical is searching for a highly motivated CRA in Germany. 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 and the position will involve frequent travelling related to monitoring visits.

• Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ISO 14155, SOPs, and regulations.
• Serve as main point of contact with the study site.
• Perform Source Data Review (SDR), Source Data Verification (SDV) and review Case Report Forms (CRFs).
• Document monitoring visits and submit reports on time.
• Handle and distribute study supplies and products, when applicable.
• Set up site budgets and agreements.
• Contribute to regulatory/CTIS and EC submissions.
• Provide training and develop study materials.

• Bachelor’s degree or equivalent in a relevant field.
• Knowledge of ICH-GCP and national regulations.
• Experience in monitoring clinical studies and site management.
• Fluent in the local language and English.
• Strong writing and IT skills.

• Service-minded with strong communication and presentation skills.
• Well-organized, able to work both independently and within teams.
• Independent, flexible, accurate, and solution oriented.
• Demonstrates initiative and adapts well to changing situations.
• Focuses on customer needs, works methodically, and achieves project goals
  consistently.
• Open to new ideas, adaptable to different people and cultures.

LINK Medical offers 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.

If you would like to know more or if you have any questions about the position, please contact Director of Clinical Operations:
Trine Dyring, trine.dyring.jensen@linkmedical.eu
Sharareh Elfversson, sharareh.elfversson@linkmedical.eu
All applications are treated confidentially and will be evaluated when received, so please apply as soon as possible. Please submit your application in English.

Last day for application: 30th of May 2025.

Please apply to the job by filling out the application below