Clinical Research Associate II
72% Flex
Offer summary
Qualifications: At least 3 years of clinical monitoring experience, Relevant life science or healthcare background, Fluency in English and local language, both written and verbal.
Key responsabilities:
- Monitor trial activities at Investigator Sites
- Track study data and prepare reports
- Maintain Trial Master File and Investigator Site File
- Attend Investigator Meetings
Job description
Required profile
Experience
Level of experience :
Junior (1-2 years)Spoken language(s)
Check out the description to know which languages are mandatory.
Soft Skills
- Strong interpersonal and organizational skills
- Attention to detail and ability to multitask effectively
- Excellent communication and client-focused mindset
- Willingness to travel up to 65%, dependent on project requirements
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