Clinical Research Associate
2 days ago
- 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 are looking forward to your application.
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