As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks
Job Summary
As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks.
Key responsibilities include maintaining and updating study documentation, supporting patient screening and enrollment, performing data entry, and communicating with study monitors.
At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science.
Matching Summary
As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks.
Skills & Requirements
Must-have
Study documentation maintenance
Patient screening and enrollment
Data entry and quality checks
Medical terminology knowledge
MS Office proficiency
Nice-to-have
Interpersonal and communication skills
Organizational skills and attention to detail
Global team advancement of healthcare
Key Requirements
Bachelor’s degree or equivalent experience
1-2 years Clinical Research Assistant/Nurse/Coordinator experience