This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA
Job Summary
This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA.
In this role, you will be involved in the process of supporting clinical trials for various therapies at the country level, and be the liaison between the site and Contract Research Organization (CRO) / Pharmaceutical Company.
Learning opportunities include comprehensive Good Clinical Practice (GCP) training, knowledge in clinical research industry, ethics, regulatory inspection readiness, and clinical trial management systems.
Matching Summary
This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA.
Skills & Requirements
Must-have
Good Clinical Practice (GCP) knowledge
Clinical Trial Management System experience
Regulatory documents management
Strong interpersonal communication skills
Proficient in MS Office applications
Attention to detail
Nice-to-have
Effective minute taking during meetings
Managing challenging communications
Cross-cultural awareness
Soft skills and technical trainings
Key Requirements
Bachelor of Science in Life Sciences or Healthcare
Good written and verbal communication skills
General awareness of clinical trial environment
Ability to establish effective working relationships