Clinical Research Associate, Sponsor-dedicated - Croatia
Ivivamedical
Croatia
On-site monitoring experience
Gcp and ich guidelines
Site selection, initiation, monitoring, close-out
Performing site selection, initiation, monitoring and close-out visits is a key responsibility
Job Summary
Performing site selection, initiation, monitoring and close-out visits is a key responsibility.
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is essential.
Collaborating with experts at study sites and with client representatives is part of the role.
Matching Summary
Performing site selection, initiation, monitoring and close-out visits is a key responsibility.
Skills & Requirements
Must-have
on-site monitoring experience
GCP and ICH guidelines
site selection, initiation, monitoring, close-out
subject recruitment plan development
tracking regulatory submissions
Croatian and English language
Nice-to-have
effective working relationships
problem-solving skills
time management skills
organizational skills
Key Requirements
At least 1 year of on-site monitoring experience
University degree in scientific discipline or health care
Good knowledge of clinical research regulatory requirements