Clinical Research Associate (CRA) / Monitor (f/m/d)

• You support project management in the planning, organisation, and implementation of national and international clinical trials in phases II to IV.
• You conduct monitor visits (initiation, monitoring of ongoing trial activities, and close-out) in accordance with SOPs and applicable guidelines across the UK.
• You work closely with the trial centers and the relevant departments of the sponsor.
• You prepare study-related documents (e.g., for authorities and ethics committees) and project plans, select potential trial centers, prepare training courses and presentations, and conduct these independently.
• You are a scientist, physician, or have a relevant qualification in the medical field.
• It would be advantageous if you already have professional experience as a CRA or have successfully completed basic CRA training.
• You have strong communication skills and fluency in English.
• Additional excellent language skills and knowledge of ICH-GCP guidelines are an advantage but not a requirement.
• You are flexible when the role requires.
• You are organised, punctual, have great interpersonal skills and happy to work with the team.
• You have an entitlement to work in the UK.
• You have a UK drivers licence.
• We ensure you a thorough introduction and support from a team of experienced natural scientists.
• We offer exciting and varied projects from the pharmaceutical, biotech and medical production sectors.
• We guarantee fast decision-making processes due to flat hierarchies and "open doors" culture.
• We love diversity! Our teams are diverse, cross-generational and we work and learn with and from each other.
• We have modern, well-equipped offices.
• We provide flexible home office options with a minimum of 1 day per week in the office.

We invite you to join us in making a lasting difference in the lives of countless patients. Every day anew.

We are looking forward to your application.