Senior Clinical Research Associate
72% Flex
Offer summary
Qualifications: At least 3 years of clinical monitoring experience, Relevant life science degree or health care background, Strong communication and organizational skills, Proficiency in English and local language.
Key responsabilities:
- Govern quality standards for trial monitoring
- Perform selection, initiation, monitoring visits at sites
- Ensure adherence to GCP, ICH, SOPs, study protocols
- Maintain Trial Master File, Investigator Site File
Job description
Required profile
Experience
Level of experience :
Mid-level (2-5 years)Industry :
Spoken language(s)
Check out the description to know which languages are mandatory.
Soft Skills
- Strong interpersonal and communication skills
- Proactive, client-focused, team player
- Attention to detail and analytical thinking
- Ability to manage multiple projects
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