MAPS European team is seeking an enthusiastic, focused, and organized Clinical Research Associates to join our Clinical Operations Department.
Suitable candidates should at the minimum:
- have 3-4 years of clinical research experience monitoring clinical studies in the Netherlands, Czech Republic, Portugal and in UK.
- Be native speakers
- Be familiar with the country specific clinical research laws and regulations
The CRA role will report to the Clinical Program Lead and will ensure that clinical trials are conducted in a timely manner and in accordance with Standard Operating Procedures (SOPs), the principles of ICH/Good Clinical Practice and all applicable regulations governing the conduct of clinical trials. Suitable candidates are able to work well in a fast environment and adept at organizing and managing lots of information virtually.
How to apply:
Interested and qualified candidates are encouraged to send their CV and motivation letter to firstname.lastname@example.org.
|Role||Freelance Clinical Research Associates (CRAs)|