Your mission
- You support the project management in terms of planning, organization and implementation of national and international clinical studies of phases II to IV.
- You conduct monitor visits (initiation, monitoring of ongoing study activities and close-out) according to SOPs as well as applicable guidelines.
- You support and cooperate closely with the trial sites as well as the corresponding 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.
Your Profile
- You have minimum 3-5 years of experience as CRA.
- You are a natural scientist, medical doctor or have a corresponding qualification in the medical field.
- You are a native speaker of Polish and have very good English language skills.
- You are confident in the use of common MS Office programs.
- You have knowledge of the ICH-GCP guidelines.
- You are characterized by team-oriented and above all structured work, are reliable, communicative, flexible and enjoy travelling.
Why us?
- 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 in the heart of Warsaw.
- We provide flexible home office options.
We invite you to join us in making a lasting difference in the lives of countless patients. Every day anew.
Interested?
We are looking forward to your application.