Experienced Clinical Research Associate Sponsor-dedicated
Ivivamedical
Good clinical practice (gcp) knowledge
International conference on harmonization guidelines
On-site monitoring experience
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice
Job Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice.
Candidates must possess at least 2 years of on-site monitoring experience and a high school diploma or equivalent degree in a scientific discipline.
The position requires proficiency in both Greek and English languages along with strong computer skills for Microsoft Office and mobile devices.
Matching Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice.
Skills & Requirements
Must-have
Good Clinical Practice (GCP) knowledge
International Conference on Harmonization guidelines
On-site monitoring experience
Greek and English language skills
Nice-to-have
Strong organizational and problem-solving skills
Effective time and financial management
Ability to establish working relationships
Key Requirements
At least 2 years of on-site monitoring experience
High School Diploma or Degree in scientific discipline