Offer summary
Qualifications:
Bachelor's degree in a scientific or healthcare-related field, Minimum of 2 years of experience as a Clinical Research Associate, In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines, Strong organizational and communication skills, Ability to work independently and collaboratively in a fast-paced environment.Key responsabilities:
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process
- Collaborate with investigators and site staff for smooth study conduct
- Perform data review and resolution of queries for high-quality clinical data
- Contribute to preparation and review of study documentation
