Experienced Clinical Research Associate Sponsor-dedicated
IQVIA UK
Riyadh, Saudi Arabia
Site monitoring visits
Protocol adherence
Regulatory requirements
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements
Job Summary
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Matching Summary
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Skills & Requirements
Must-have
site monitoring visits
protocol adherence
regulatory requirements
subject recruitment plan
Good Clinical Practice
ICH guidelines
Nice-to-have
effective time management
problem-solving skills
client relationship management
therapeutic knowledge
Key Requirements
at least 2 years on-site monitoring experience
High School Diploma or equivalent
Degree in scientific discipline or health care preferred
Good knowledge of applicable clinical research regulatory requirements
Proficiency in Microsoft Word, Excel and PowerPoint